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Pediatric Disease Annotations & Medicines



   crohn disease
  

Disease ID 39
Disease crohn disease
Definition
A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the COLON. In Crohn disease, the inflammation, extending through the intestinal wall from the MUCOSA to the serosa, is characteristically asymmetric and segmental. Epithelioid GRANULOMAS may be seen in some patients.
Synonym
-- crohn's disease
cd - crohn's disease
crohn dis
crohn disease [disease/finding]
crohn diseases
crohn s
crohn s disease
crohn's
crohn's disease
crohn's disease (disorder)
crohn's disease nos
crohn's disease, nos
crohn's diseases
crohn's enteritis
crohn's regional enteritis
crohns dis
crohns disease
crohns diseases
crohns's
crohns's disease
disease crohn
disease crohn's
disease crohns
eleocolitis
enteritis (regional)
enteritis regional
granulomatous enteritis
granulomatous enteritis and colitis
granulomatous enteritis, nos
ibd1
inflammatory bowel disease (crohn disease) 1
inflammatory bowel disease 1
inflammatory bowel disease, regional enteritis
morbus crohn
re - regional enteritis
regional enteritis
regional enteritis (crohn's disease)
regional enteritis - crohn
regional enteritis - crohn's disease
regional enteritis, nos
OMIM
DOID
UMLS
C0010346
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:269)
C0021831  |  bowel disease  |  30
C0021390  |  inflammatory bowel disease  |  23
C0009319  |  colitis  |  22
C0009324  |  ulcerative colitis  |  13
C0030524  |  paratuberculosis  |  11
C0024299  |  lymphoma  |  11
C0042384  |  vasculitis  |  9
C0001418  |  adenocarcinoma  |  8
C0002871  |  anemia  |  7
C0034212  |  pyoderma  |  7
C0002726  |  amyloidosis  |  7
C0009402  |  colorectal cancer  |  6
C0033860  |  psoriasis  |  6
C0008313  |  sclerosing cholangitis  |  6
C0040053  |  thrombosis  |  6
C0566602  |  primary sclerosing cholangitis  |  6
C0011991  |  diarrhea  |  6
C0007113  |  rectal cancer  |  6
C0003864  |  arthritis  |  6
C0019348  |  herpes simplex  |  5
C0021390  |  inflammatory bowel diseases  |  5
C0021843  |  bowel obstruction  |  5
C0085652  |  pyoderma gangrenosum  |  5
C0008311  |  cholangitis  |  5
C0019158  |  hepatitis  |  5
C0029443  |  osteomyelitis  |  4
C0039263  |  takayasu's arteritis  |  4
C0021843  |  intestinal obstruction  |  4
C0442874  |  neuropathy  |  4
C0010414  |  cryptococcosis  |  4
C0017661  |  iga nephropathy  |  4
C0023418  |  leukemia  |  4
C0024141  |  systemic lupus erythematosus  |  4
C0001339  |  acute pancreatitis  |  4
C0409974  |  lupus erythematosus  |  4
C0030305  |  pancreatitis  |  4
C0022658  |  nephropathy  |  4
C0021845  |  bowel perforation  |  3
C0003873  |  rheumatoid arthritis  |  3
C0042900  |  vitiligo  |  3
C0085160  |  hidradenitis  |  3
C0037198  |  sinus thrombosis  |  3
C0018202  |  granulomatous vasculitis  |  3
C0032285  |  pneumonia  |  3
C0023524  |  progressive multifocal leukoencephalopathy  |  3
C0032285  |  pneumonitis  |  3
C0270612  |  leukoencephalopathy  |  3
C0041296  |  tuberculosis  |  3
C0155223  |  dacryoadenitis  |  3
C1258215  |  ileus  |  3
C0343386  |  clostridium difficile infection  |  3
C0020875  |  ileal disease  |  3
C0036202  |  sarcoidosis  |  3
C0276688  |  pulmonary cryptococcosis  |  3
C0035258  |  restless legs syndrome  |  3
C0028754  |  obesity  |  3
C0035258  |  restless legs  |  3
C0016412  |  folate deficiency  |  3
C0029456  |  osteoporosis  |  3
C0011570  |  depression  |  3
C0003509  |  aortitis  |  2
C0025162  |  toxic megacolon  |  2
C0019829  |  hodgkin's lymphoma  |  2
C0027813  |  neuritis  |  2
C0029134  |  optic neuritis  |  2
C0553662  |  juvenile idiopathic arthritis  |  2
C0013298  |  duodenitis  |  2
C0027726  |  nephrotic syndrome  |  2
C0341335  |  cmv colitis  |  2
C0021831  |  enteropathy  |  2
C0021831  |  intestinal disease  |  2
C0025160  |  megacolon  |  2
C0007102  |  colon cancer  |  2
C0162429  |  malnutrition  |  2
C0162836  |  hidradenitis suppurativa  |  2
C0025289  |  meningitis  |  2
C0015230  |  rash  |  2
C0008350  |  gallstone  |  2
C0041321  |  miliary tuberculosis  |  2
C0021933  |  intussusception  |  2
C0042870  |  vitamin d deficiency  |  2
C0024523  |  malabsorption  |  2
C0030312  |  pancytopenia  |  2
C0009447  |  common variable immunodeficiency  |  2
C0008350  |  gallstones  |  2
C0017152  |  gastritis  |  2
C0007570  |  celiac disease  |  2
C0949691  |  spondyloarthropathy  |  2
C0019829  |  hodgkin lymphoma  |  2
C0007113  |  rectal carcinoma  |  2
C0023467  |  acute myeloid leukemia  |  2
C0040053  |  thrombus  |  2
C0018203  |  chronic granulomatous disease  |  2
C0040034  |  thrombocytopenia  |  2
C0022568  |  keratitis  |  2
C0030920  |  peptic ulcer  |  2
C0868908  |  pancolitis  |  2
C0042870  |  vitamin d defic  |  2
C0018021  |  goiter  |  2
C0026718  |  mucormycosis  |  2
C0031154  |  peritonitis  |  2
C0027121  |  myositis  |  2
C0023470  |  myeloid leukemia  |  2
C0031090  |  periodontal disease  |  2
C0019204  |  hepatocellular carcinoma  |  2
C0003467  |  anxiety  |  2
C0162429  |  nutritional deficiencies  |  1
C0014527  |  epidermolysis bullosa  |  1
C0038362  |  stomatitis  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0023827  |  liposarcoma  |  1
C0019360  |  herpes zoster  |  1
C0023895  |  liver disease  |  1
C0949690  |  spondyloarthritis  |  1
C0034150  |  purpura  |  1
C0034065  |  pulmonary embolism  |  1
C0022104  |  irritable bowel  |  1
C0022806  |  kwashiorkor  |  1
C0334254  |  lymphoepithelioma  |  1
C0023418  |  leukaemia  |  1
C0024314  |  lymphoproliferative disorders  |  1
C0021390  |  irritable bowel disease  |  1
C0026769  |  multiple sclerosis  |  1
C0178238  |  intestinal infection  |  1
C0001418  |  adenocarcinomas  |  1
C0004030  |  aspergillosis  |  1
C0007137  |  squamous cell carcinoma  |  1
C0002878  |  hemolytic anemia  |  1
C0238463  |  papillary thyroid carcinoma  |  1
C0017178  |  gastrointestinal disorder  |  1
C0030524  |  johne's disease  |  1
C0042721  |  virus hepatitis  |  1
C0026946  |  fungal infection  |  1
C0005741  |  blepharitis  |  1
C0019163  |  hepatitis b  |  1
C0699790  |  colon carcinoma  |  1
C0025037  |  meckel's diverticulum  |  1
C0024291  |  hemophagocytic lymphohistiocytosis  |  1
C0022116  |  ischemia  |  1
C0031069  |  familial mediterranean fever  |  1
C0011334  |  cavities  |  1
C0037274  |  skin diseases  |  1
C0393819  |  chronic inflammatory demyelinating polyradiculoneuropathy  |  1
C0346627  |  intestinal cancers  |  1
C0041331  |  splenic tuberculosis  |  1
C0085253  |  adult onset still's disease  |  1
C0037274  |  dermatosis  |  1
C0008312  |  biliary cirrhosis  |  1
C0018920  |  cavernoma  |  1
C0032305  |  pneumocystis jiroveci pneumonia  |  1
C0024299  |  malignant lymphoma  |  1
C0024299  |  malignant lymphomas  |  1
C0024205  |  lymphadenitis  |  1
C0023487  |  acute promyelocytic leukaemia  |  1
C0023448  |  lymphoblastic leukemia  |  1
C0270629  |  epidural abscess  |  1
C0031099  |  periodontitis  |  1
C0007104  |  carcinoma of the breast  |  1
C0751878  |  central nervous system vasculitis  |  1
C0030805  |  pemphigoid  |  1
C0039263  |  takayasu's disease  |  1
C0009402  |  colorectal carcinoma  |  1
C0035078  |  kidney failure  |  1
C0037274  |  dermatoses  |  1
C0002880  |  autoimmune hemolytic anemia  |  1
C0036992  |  short bowel syndrome  |  1
C0003615  |  appendicitis  |  1
C0003125  |  anorexia nervosa  |  1
C0019348  |  herpes simplex infection  |  1
C0028756  |  morbid obesity  |  1
C0008312  |  primary biliary cirrhosis  |  1
C0085655  |  polymyositis  |  1
C0024440  |  cystoid macular oedema  |  1
C0011854  |  type 1 diabetes  |  1
C0035854  |  rosacea  |  1
C0004943  |  behcet's disease  |  1
C0023890  |  cirrhosis  |  1
C0038220  |  status epilepticus  |  1
C0042769  |  viral infection  |  1
C0036416  |  scleritis  |  1
C0279637  |  carcinoma of the anus  |  1
C0006625  |  cachectic  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0029132  |  optic neuropathy  |  1
C0024214  |  lymphangiectasia  |  1
C1527336  |  sjogren's syndrome  |  1
C0031117  |  peripheral neuropathy  |  1
C0162293  |  papillitis  |  1
C0025290  |  aseptic meningitis  |  1
C0002871  |  anemias  |  1
C0001430  |  adenoma  |  1
C0014236  |  endophthalmitis  |  1
C0598608  |  hyperhomocysteinemia  |  1
C0038041  |  spotted fever  |  1
C0026946  |  fungal infections  |  1
C0376175  |  bell's palsy  |  1
C0751711  |  anterior ischemic optic neuropathy  |  1
C0005940  |  bone disease  |  1
C0043117  |  idiopathic thrombocytopenic purpura  |  1
C0079293  |  epidermolysis bullosa acquisita  |  1
C0024299  |  lymphomas  |  1
C0017919  |  glycogen storage disease  |  1
C0032305  |  pneumocystis  |  1
C0002991  |  dermatofibroma  |  1
C0017178  |  gastrointestinal disorders  |  1
C0017661  |  iga glomerulonephritis  |  1
C0024221  |  lymphangioma  |  1
C0392525  |  nephrolithiasis  |  1
C0085167  |  granular cell tumour  |  1
C1412036  |  squamous cell carcinoma of the anus  |  1
C0032305  |  pneumocystosis  |  1
C0035309  |  retinopathy  |  1
C0022893  |  labyrinthitis  |  1
C0039446  |  telangiectasia  |  1
C0012739  |  disseminated intravascular coagulation  |  1
C0020877  |  ileitis  |  1
C0043092  |  wegener's granulomatosis  |  1
C0003874  |  septic arthritis  |  1
C0007113  |  carcinoma of the rectum  |  1
C0221036  |  acrodermatitis enteropathica  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0005586  |  bipolar disorder  |  1
C0037274  |  skin disease  |  1
C0003872  |  psoriatic arthritis  |  1
C0021831  |  intestinal diseases  |  1
C0007115  |  thyroid ca  |  1
C0019655  |  histoplasmosis  |  1
C0002438  |  amoebiasis  |  1
C0024236  |  lymphedema  |  1
C0339962  |  pulmonary mucormycosis  |  1
C0011226  |  hepatitis d  |  1
C0014118  |  endocarditis  |  1
C0043117  |  immune thrombocytopenic purpura  |  1
C0027697  |  nephritis  |  1
C0033687  |  proteinuria  |  1
C0032587  |  polyradiculoneuropathy  |  1
C0018916  |  angioma  |  1
C0017105  |  gas gangrene  |  1
C0042769  |  virus infection  |  1
C0033680  |  protein losing enteropathy  |  1
C0036114  |  salmonellosis  |  1
C0079774  |  peripheral t-cell lymphoma  |  1
C0019196  |  hepatitis c  |  1
C0035258  |  restless legs syndrome (rls)  |  1
C0025202  |  malignant melanoma  |  1
C0024312  |  lymphopenia  |  1
C0017658  |  glomerulonephritis  |  1
C0410422  |  chronic recurrent multifocal osteomyelitis  |  1
C0022660  |  acute kidney failure  |  1
C0028242  |  nocardiosis  |  1
C0009806  |  constipation  |  1
C0027707  |  interstitial nephritis  |  1
C0039445  |  hereditary hemorrhagic telangiectasia  |  1
C0004245  |  atrioventricular block  |  1
C0027831  |  von recklinghausen disease  |  1
C0019360  |  zoster  |  1
C0006060  |  mediterranean spotted fever  |  1
C0029442  |  osteomalacia  |  1
C0017105  |  clostridial myonecrosis  |  1
C0014541  |  epiglottitis  |  1
C0011847  |  diabetes  |  1
C0549473  |  thyroid carcinoma  |  1
C0039263  |  takayasu disease  |  1
C0151436  |  leukocytoclastic vasculitis  |  1
C0025309  |  meningoencephalitis  |  1
C0005745  |  ptosis  |  1
C0041316  |  tuberculous lymphadenitis  |  1
C0025202  |  melanoma  |  1
C0026393  |  molluscum contagiosum  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:102)
HLA-DRB1  |  3123  |  CTD_human
TNF  |  7124  |  CTD_human;GWASCAT
IL6  |  3569  |  CTD_human
BACH2  |  60468  |  CTD_human;GWASCAT
STAT3  |  6774  |  GWASCAT
GPR65  |  8477  |  GWASCAT
SMAD3  |  4088  |  CTD_human;GWASCAT
IFNG  |  3458  |  CTD_human
LEP  |  3952  |  CTD_human
ADIPOQ  |  9370  |  CTD_human
NOD2  |  64127  |  CTD_human;GWASCAT;GHR
CRP  |  1401  |  CTD_human
DNMT3A  |  1788  |  CTD_human;GWASCAT
CCL2  |  6347  |  CTD_human
THADA  |  63892  |  GWASCAT
PPARA  |  5465  |  CTD_human
C1orf106  |  55765  |  GWASCAT
CLN3  |  1201  |  GWASCAT
SOCS1  |  8651  |  GWASCAT
BTNL2  |  56244  |  GWASCAT
C21orf33  |  8209  |  GWASCAT
PHTF1  |  10745  |  GWASCAT
IL12B  |  3593  |  CTD_human
TYK2  |  7297  |  CTD_human;GWASCAT
PTPN22  |  26191  |  GWASCAT
UBE2L3  |  7332  |  GWASCAT
NR1H4  |  9971  |  CTD_human
PHOX2B  |  8929  |  CTD_human
GCKR  |  2646  |  GWASCAT
ANKRD55  |  79722  |  GWASCAT
MST1  |  4485  |  CTD_human;GWASCAT
IL23R  |  149233  |  CTD_human;GWASCAT;GHR
IL2RA  |  3559  |  CTD_human;GWASCAT
FGFR1OP  |  11116  |  GWASCAT
BANK1  |  55024  |  GWASCAT
IGF1  |  3479  |  CTD_human
IL10  |  3586  |  CTD_human
PPARG  |  5468  |  CTD_human
SP140  |  11262  |  GWASCAT
NLRP3  |  114548  |  CTD_human
CCNY  |  219771  |  CTD_human;GWASCAT
FUT2  |  2524  |  CTD_human;GWASCAT
SLC11A1  |  6556  |  CTD_human
PSMB10  |  5699  |  GWASCAT
ZGPAT  |  84619  |  GWASCAT
SBSPON  |  157869  |  GWASCAT
TAGAP  |  117289  |  CTD_human
LACC1  |  144811  |  GWASCAT
PPP5C  |  5536  |  GWASCAT
C5orf56  |  441108  |  GWASCAT
PTPN2  |  5771  |  CTD_human;GWASCAT
TLR4  |  7099  |  CTD_human
LTA  |  4049  |  GWASCAT
SLC22A23  |  63027  |  GWASCAT
CPEB4  |  80315  |  GWASCAT
NCF4  |  4689  |  CTD_human
TMEM258  |  746  |  GWASCAT
ITLN1  |  55600  |  GWASCAT
ZNF365  |  22891  |  GWASCAT
IRGM  |  345611  |  CTD_human;GHR
DENND1B  |  163486  |  CTD_human;GWASCAT
PSORS1C3  |  100130889  |  GWASCAT
FAM92B  |  339145  |  CTD_human
PTRF  |  284119  |  GWASCAT
VTN  |  7448  |  CTD_human
C1orf141  |  400757  |  GWASCAT
PUS10  |  150962  |  GWASCAT
JAZF1  |  221895  |  GWASCAT
CD244  |  51744  |  GWASCAT
ATG16L1  |  55054  |  CTD_human;GWASCAT;GHR
GPBAR1  |  151306  |  CTD_human
MLN  |  4295  |  GWASCAT
NKX2-3  |  159296  |  CTD_human;GWASCAT
ZMIZ1  |  57178  |  GWASCAT
PER3  |  8863  |  GWASCAT
ERAP2  |  64167  |  CTD_human;GWASCAT
TNFSF15  |  9966  |  GWASCAT
SCAMP3  |  10067  |  GWASCAT
CARD9  |  64170  |  GWASCAT
BSN  |  8927  |  GWASCAT
IFNGR2  |  3460  |  GWASCAT
FN1  |  2335  |  CTD_human
SKAP2  |  8935  |  GWASCAT
TLR9  |  54106  |  CTD_human
MUC19  |  283463  |  GWASCAT
ELF1  |  1997  |  GWASCAT
IL18RAP  |  8807  |  GWASCAT
LINC00492  |  100861468  |  GWASCAT
CLCA2  |  9635  |  GWASCAT
CDKAL1  |  54901  |  GWASCAT
SLAIN2  |  57606  |  GWASCAT
LINC01475  |  101927324  |  GWASCAT
KSR1  |  8844  |  GWASCAT
SCARNA5  |  677775  |  GWASCAT
RSPO3  |  84870  |  GWASCAT
FCHSD2  |  9873  |  GWASCAT
MAGI1  |  9223  |  GWASCAT
FPR2  |  2358  |  CTD_human
SBNO2  |  22904  |  GWASCAT
MROH3P  |  647215  |  GWASCAT
TMEM17  |  200728  |  GWASCAT
RNASET2  |  8635  |  GWASCAT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:150)
5243  |  ABCB1  |  infer
55054  |  ATG16L1  |  infer
10678  |  B3GNT2  |  infer
60468  |  BACH2  |  infer
91272  |  BOD1  |  infer
8927  |  BSN  |  infer
256815  |  C10orf67  |  infer
8209  |  C21orf33  |  infer
441108  |  C5orf56  |  infer
100130988  |  C7orf72  |  infer
64170  |  CARD9  |  infer
842  |  CASP9  |  infer
6347  |  CCL2  |  infer
54901  |  CDKAL1  |  infer
1201  |  CLN3  |  infer
26047  |  CNTNAP2  |  infer
1601  |  DAB2  |  infer
1672  |  DEFB1  |  infer
163486  |  DENND1B  |  infer
9231  |  DLG5  |  infer
1788  |  DNMT3A  |  infer
64167  |  ERAP2  |  infer
56677  |  FABP3P2  |  infer
356  |  FASLG  |  infer
2214  |  FCGR3A  |  infer
11116  |  FGFR1OP  |  infer
2524  |  FUT2  |  infer
2646  |  GCKR  |  infer
2805  |  GOT1  |  infer
8477  |  GPR65  |  infer
3119  |  HLA-DQB1  |  infer
50941  |  IBD5  |  infer
340198  |  IFITM4P  |  infer
3500  |  IGHG1  |  infer
3586  |  IL10  |  infer
3593  |  IL12B  |  infer
8807  |  IL18RAP  |  infer
149233  |  IL23R  |  infer
3559  |  IL2RA  |  infer
3562  |  IL3  |  infer
3569  |  IL6  |  infer
345611  |  IRGM  |  infer
55600  |  ITLN1  |  infer
1316  |  KLF6  |  infer
134008  |  MRPL11P2  |  infer
359779  |  MRPS35P3  |  infer
4485  |  MST1  |  infer
4524  |  MTHFR  |  infer
4548  |  MTR  |  infer
4552  |  MTRR  |  infer
4650  |  MYO9B  |  infer
4745  |  NELL1  |  infer
79576  |  NKAP  |  infer
159296  |  NKX2-3  |  infer
10392  |  NOD1  |  infer
64127  |  NOD2  |  infer
2908  |  NR3C1  |  infer
8204  |  NRIP1  |  infer
5155  |  PDGFB  |  infer
8863  |  PER3  |  infer
5334  |  PLCL1  |  infer
5468  |  PPARG  |  infer
25824  |  PRDX5  |  infer
5699  |  PSMB10  |  infer
56984  |  PSMG2  |  infer
26191  |  PTPN22  |  infer
150962  |  PUS10  |  infer
5820  |  PVT1  |  infer
10171  |  RCL1  |  infer
326275  |  RPL12P7  |  infer
100271305  |  RPL30P13  |  infer
728010  |  RPL35P3  |  infer
100271352  |  RPS12P16  |  infer
100271063  |  RPS14P1  |  infer
100271600  |  RPS3AP51  |  infer
6304  |  SATB1  |  infer
10067  |  SCAMP3  |  infer
63027  |  SLC22A23  |  infer
6583  |  SLC22A4  |  infer
6584  |  SLC22A5  |  infer
29015  |  SLC43A3  |  infer
56301  |  SLC7A10  |  infer
133482  |  SLCO6A1  |  infer
4088  |  SMAD3  |  infer
11262  |  SP140  |  infer
6774  |  STAT3  |  infer
117289  |  TAGAP  |  infer
256536  |  TCERG1L  |  infer
63892  |  THADA  |  infer
134288  |  TMEM174  |  infer
7124  |  TNF  |  infer
7132  |  TNFRSF1A  |  infer
7133  |  TNFRSF1B  |  infer
9966  |  TNFSF15  |  infer
10221  |  TRIB1  |  infer
7297  |  TYK2  |  infer
7332  |  UBE2L3  |  infer
84619  |  ZGPAT  |  infer
57178  |  ZMIZ1  |  infer
22891  |  ZNF365  |  infer
124626  |  ZPBP2  |  infer
219771  |  CCNY  |  infer
5771  |  PTPN2  |  infer
729230  |  CCR2  |  infer
1234  |  CCR5  |  infer
1235  |  CCR6  |  infer
929  |  CD14  |  infer
930  |  CD19  |  infer
1401  |  CRP  |  infer
1436  |  CSF1R  |  infer
1543  |  CYP1A1  |  infer
2052  |  EPHX1  |  infer
2944  |  GSTM1  |  infer
2950  |  GSTP1  |  infer
2952  |  GSTT1  |  infer
3106  |  HLA-B  |  infer
3122  |  HLA-DRA  |  infer
3123  |  HLA-DRB1  |  infer
3304  |  HSPA1B  |  infer
3306  |  HSPA2  |  infer
3383  |  ICAM1  |  infer
23308  |  ICOSLG  |  infer
3603  |  IL16  |  infer
3606  |  IL18  |  infer
3554  |  IL1R1  |  infer
3565  |  IL4  |  infer
3566  |  IL4R  |  infer
3659  |  IRF1  |  infer
3717  |  JAK2  |  infer
120892  |  LRRK2  |  infer
4049  |  LTA  |  infer
4153  |  MBL2  |  infer
4282  |  MIF  |  infer
283463  |  MUC19  |  infer
4790  |  NFKB1  |  infer
4792  |  NFKBIA  |  infer
94103  |  ORMDL3  |  infer
5027  |  P2RX7  |  infer
8974  |  P4HA2  |  infer
9124  |  PDLIM1  |  infer
170679  |  PSORS1C1  |  infer
5734  |  PTGER4  |  infer
5054  |  SERPINE1  |  infer
6556  |  SLC11A1  |  infer
7097  |  TLR2  |  infer
7099  |  TLR4  |  infer
54106  |  TLR9  |  infer
7172  |  TPMT  |  infer
7421  |  VDR  |  infer
1610  |  DAO  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:757)
100419743  |  DBET  |  DISEASES
2288  |  FKBP4  |  DISEASES
6542  |  SLC7A2  |  DISEASES
10344  |  CCL26  |  DISEASES
6376  |  CX3CL1  |  DISEASES
8993  |  PGLYRP1  |  DISEASES
920  |  CD4  |  DISEASES
3385  |  ICAM3  |  DISEASES
7132  |  TNFRSF1A  |  DISEASES
602  |  BCL3  |  DISEASES
8974  |  P4HA2  |  DISEASES
6694  |  SPP2  |  DISEASES
3566  |  IL4R  |  DISEASES
6343  |  SCT  |  DISEASES
30009  |  TBX21  |  DISEASES
1361  |  CPB2  |  DISEASES
4680  |  CEACAM6  |  DISEASES
6583  |  SLC22A4  |  DISEASES
6583  |  SLC22A4  |  DISEASES
1725  |  DHPS  |  DISEASES
8174  |  MADCAM1  |  DISEASES
4282  |  MIF  |  DISEASES
6948  |  TCN2  |  DISEASES
3956  |  LGALS1  |  DISEASES
7494  |  XBP1  |  DISEASES
3162  |  HMOX1  |  DISEASES
158  |  ADSL  |  DISEASES
11035  |  RIPK3  |  DISEASES
1511  |  CTSG  |  DISEASES
3002  |  GZMB  |  DISEASES
4792  |  NFKBIA  |  DISEASES
3929  |  LBP  |  DISEASES
7076  |  TIMP1  |  DISEASES
479  |  ATP12A  |  DISEASES
54602  |  NDFIP2  |  DISEASES
2862  |  MLNR  |  DISEASES
4313  |  MMP2  |  DISEASES
4210  |  MEFV  |  DISEASES
343  |  AQP8  |  DISEASES
55192  |  DNAJC17  |  DISEASES
8767  |  RIPK2  |  DISEASES
10404  |  CPQ  |  DISEASES
8797  |  TNFRSF10A  |  DISEASES
4051  |  CYP4F3  |  DISEASES
56729  |  RETN  |  DISEASES
7040  |  TGFB1  |  DISEASES
973  |  CD79A  |  DISEASES
1048  |  CEACAM5  |  DISEASES
57817  |  HAMP  |  DISEASES
10061  |  ABCF2  |  DISEASES
3912  |  LAMB1  |  DISEASES
10392  |  NOD1  |  DISEASES
10392  |  NOD1  |  DISEASES
6369  |  CCL24  |  DISEASES
5054  |  SERPINE1  |  DISEASES
944  |  TNFSF8  |  DISEASES
6348  |  CCL3  |  DISEASES
4353  |  MPO  |  DISEASES
8288  |  EPX  |  DISEASES
1440  |  CSF3  |  DISEASES
6347  |  CCL2  |  DISEASES
6357  |  CCL13  |  DISEASES
1277  |  COL1A1  |  DISEASES
7448  |  VTN  |  DISEASES
6372  |  CXCL6  |  DISEASES
8929  |  PHOX2B  |  DISEASES
4790  |  NFKB1  |  DISEASES
3558  |  IL2  |  DISEASES
24145  |  PANX1  |  DISEASES
3587  |  IL10RA  |  DISEASES
969  |  CD69  |  DISEASES
51561  |  IL23A  |  DISEASES
55801  |  IL26  |  DISEASES
3458  |  IFNG  |  DISEASES
3820  |  KLRB1  |  DISEASES
1432  |  MAPK14  |  DISEASES
2690  |  GHR  |  DISEASES
3565  |  IL4  |  DISEASES
3567  |  IL5  |  DISEASES
2908  |  NR3C1  |  DISEASES
6556  |  SLC11A1  |  DISEASES
92840  |  REEP6  |  DISEASES
5967  |  REG1A  |  DISEASES
3488  |  IGFBP5  |  DISEASES
4759  |  NEU2  |  DISEASES
3554  |  IL1R1  |  DISEASES
8809  |  IL18R1  |  DISEASES
566  |  AZU1  |  DISEASES
5657  |  PRTN3  |  DISEASES
9528  |  TMEM59  |  DISEASES
11126  |  CD160  |  DISEASES
6402  |  SELL  |  DISEASES
7276  |  TTR  |  DISEASES
7128  |  TNFAIP3  |  DISEASES
80306  |  MED28  |  DISEASES
23307  |  FKBP15  |  DISEASES
54812  |  AFTPH  |  DISEASES
4360  |  MRC1  |  DISEASES
8600  |  TNFSF11  |  DISEASES
4852  |  NPY  |  DISEASES
35  |  ACADS  |  DISEASES
7130  |  TNFAIP6  |  DISEASES
5266  |  PI3  |  DISEASES
27189  |  IL17C  |  DISEASES
54210  |  TREM1  |  DISEASES
4502  |  MT2A  |  DISEASES
6555  |  SLC10A2  |  DISEASES
6584  |  SLC22A5  |  DISEASES
6584  |  SLC22A5  |  DISEASES
3659  |  IRF1  |  DISEASES
30833  |  NT5C  |  DISEASES
718  |  C3  |  DISEASES
1236  |  CCR7  |  DISEASES
3306  |  HSPA2  |  DISEASES
7429  |  VIL1  |  DISEASES
2952  |  GSTT1  |  DISEASES
968  |  CD68  |  DISEASES
6351  |  CCL4  |  DISEASES
1215  |  CMA1  |  DISEASES
9459  |  ARHGEF6  |  DISEASES
3630  |  INS  |  DISEASES
120400  |  NXPE1  |  DISEASES
9945  |  GFPT2  |  DISEASES
6382  |  SDC1  |  DISEASES
1401  |  CRP  |  DISEASES
8546  |  AP3B1  |  DISEASES
1116  |  CHI3L1  |  DISEASES
3845  |  KRAS  |  DISEASES
759  |  CA1  |  DISEASES
27299  |  ADAMDEC1  |  DISEASES
83998  |  REG4  |  DISEASES
60468  |  BACH2  |  DISEASES
4907  |  NT5E  |  DISEASES
9038  |  TAAR5  |  DISEASES
80896  |  NPL  |  DISEASES
80896  |  NPL  |  DISEASES
55270  |  NUDT15  |  DISEASES
3569  |  IL6  |  DISEASES
10241  |  CALCOCO2  |  DISEASES
3557  |  IL1RN  |  DISEASES
26525  |  IL36RN  |  DISEASES
6366  |  CCL21  |  DISEASES
10850  |  CCL27  |  DISEASES
7097  |  TLR2  |  DISEASES
10068  |  IL18BP  |  DISEASES
4316  |  MMP7  |  DISEASES
2984  |  GUCY2C  |  DISEASES
11213  |  IRAK3  |  DISEASES
4069  |  LYZ  |  DISEASES
23359  |  FAM189A1  |  DISEASES
29121  |  CLEC2D  |  DISEASES
7450  |  VWF  |  DISEASES
7188  |  TRAF5  |  DISEASES
51444  |  RNF138  |  DISEASES
999  |  CDH1  |  DISEASES
54825  |  CDHR2  |  DISEASES
4092  |  SMAD7  |  DISEASES
4087  |  SMAD2  |  DISEASES
945  |  CD33  |  DISEASES
3595  |  IL12RB2  |  DISEASES
9618  |  TRAF4  |  DISEASES
9739  |  SETD1A  |  DISEASES
495  |  ATP4A  |  DISEASES
23031  |  MAST3  |  DISEASES
671  |  BPI  |  DISEASES
25939  |  SAMHD1  |  DISEASES
3783  |  KCNN4  |  DISEASES
5595  |  MAPK3  |  DISEASES
1326  |  MAP3K8  |  DISEASES
3682  |  ITGAE  |  DISEASES
1  |  A1BG  |  DISEASES
23523  |  CABIN1  |  DISEASES
55686  |  MREG  |  DISEASES
27178  |  IL37  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
9466  |  IL27RA  |  DISEASES
54776  |  PPP1R12C  |  DISEASES
1991  |  ELANE  |  DISEASES
6403  |  SELP  |  DISEASES
3574  |  IL7  |  DISEASES
943  |  TNFRSF8  |  DISEASES
4162  |  MCAM  |  DISEASES
3938  |  LCT  |  DISEASES
8540  |  AGPS  |  DISEASES
941  |  CD80  |  DISEASES
59067  |  IL21  |  DISEASES
2247  |  FGF2  |  DISEASES
84162  |  KIAA1109  |  DISEASES
3589  |  IL11  |  DISEASES
3589  |  IL11  |  DISEASES
6774  |  STAT3  |  DISEASES
5443  |  POMC  |  DISEASES
7297  |  TYK2  |  DISEASES
3383  |  ICAM1  |  DISEASES
7535  |  ZAP70  |  DISEASES
3827  |  KNG1  |  DISEASES
7416  |  VDAC1  |  DISEASES
5243  |  ABCB1  |  DISEASES
11234  |  HPS5  |  DISEASES
7078  |  TIMP3  |  DISEASES
939  |  CD27  |  DISEASES
55089  |  SLC38A4  |  DISEASES
3695  |  ITGB7  |  DISEASES
8477  |  GPR65  |  DISEASES
2252  |  FGF7  |  DISEASES
3687  |  ITGAX  |  DISEASES
10261  |  IGSF6  |  DISEASES
3394  |  IRF8  |  DISEASES
54849  |  DEF8  |  DISEASES
6687  |  SPG7  |  DISEASES
7157  |  TP53  |  DISEASES
6455  |  SH3GL1  |  DISEASES
207  |  AKT1  |  DISEASES
2212  |  FCGR2A  |  DISEASES
52  |  ACP1  |  DISEASES
8446  |  DUSP11  |  DISEASES
26154  |  ABCA12  |  DISEASES
2169  |  FABP2  |  DISEASES
54901  |  CDKAL1  |  DISEASES
222663  |  SCUBE3  |  DISEASES
2768  |  GNA12  |  DISEASES
7552  |  ZNF711  |  DISEASES
3934  |  LCN2  |  DISEASES
133  |  ADM  |  DISEASES
6768  |  ST14  |  DISEASES
3606  |  IL18  |  DISEASES
112936  |  VPS26B  |  DISEASES
7082  |  TJP1  |  DISEASES
7292  |  TNFSF4  |  DISEASES
5741  |  PTH  |  DISEASES
23643  |  LY96  |  DISEASES
760  |  CA2  |  DISEASES
29761  |  USP25  |  DISEASES
10  |  NAT2  |  DISEASES
10538  |  BATF  |  DISEASES
9073  |  CLDN8  |  DISEASES
6750  |  SST  |  DISEASES
5468  |  PPARG  |  DISEASES
3815  |  KIT  |  DISEASES
171586  |  ABHD3  |  DISEASES
909  |  CD1A  |  DISEASES
50848  |  F11R  |  DISEASES
3588  |  IL10RB  |  DISEASES
6781  |  STC1  |  DISEASES
114771  |  PGLYRP3  |  DISEASES
1636  |  ACE  |  DISEASES
5681  |  PSKH1  |  DISEASES
7032  |  TFF2  |  DISEASES
7031  |  TFF1  |  DISEASES
2220  |  FCN2  |  DISEASES
729230  |  CCR2  |  DISEASES
1234  |  CCR5  |  DISEASES
221914  |  GPC2  |  DISEASES
150223  |  YDJC  |  DISEASES
114757  |  CYGB  |  DISEASES
6352  |  CCL5  |  DISEASES
6777  |  STAT5B  |  DISEASES
1990  |  CELA1  |  DISEASES
58191  |  CXCL16  |  DISEASES
9965  |  FGF19  |  DISEASES
7412  |  VCAM1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
5966  |  REL  |  DISEASES
151354  |  FAM84A  |  DISEASES
27306  |  HPGDS  |  DISEASES
84666  |  RETNLB  |  DISEASES
213  |  ALB  |  DISEASES
2921  |  CXCL3  |  DISEASES
6374  |  CXCL5  |  DISEASES
5473  |  PPBP  |  DISEASES
5196  |  PF4  |  DISEASES
84343  |  HPS3  |  DISEASES
7349  |  UCN  |  DISEASES
4486  |  MST1R  |  DISEASES
308  |  ANXA5  |  DISEASES
132612  |  ADAD1  |  DISEASES
3600  |  IL15  |  DISEASES
51752  |  ERAP1  |  DISEASES
7098  |  TLR3  |  DISEASES
1437  |  CSF2  |  DISEASES
116379  |  IL22RA2  |  DISEASES
221955  |  DAGLB  |  DISEASES
10569  |  SLU7  |  DISEASES
54882  |  ANKHD1  |  DISEASES
4982  |  TNFRSF11B  |  DISEASES
1671  |  DEFA6  |  DISEASES
1672  |  DEFB1  |  DISEASES
157724  |  SLC7A13  |  DISEASES
79937  |  CNTNAP3  |  DISEASES
4783  |  NFIL3  |  DISEASES
283209  |  PGM2L1  |  DISEASES
5267  |  SERPINA4  |  DISEASES
120892  |  LRRK2  |  DISEASES
79803  |  HPS6  |  DISEASES
79158  |  GNPTAB  |  DISEASES
5896  |  RAG1  |  DISEASES
338339  |  CLEC4D  |  DISEASES
4314  |  MMP3  |  DISEASES
290  |  ANPEP  |  DISEASES
6778  |  STAT6  |  DISEASES
6778  |  STAT6  |  DISEASES
5245  |  PHB  |  DISEASES
64127  |  NOD2  |  DISEASES
64127  |  NOD2  |  DISEASES
4218  |  RAB8A  |  DISEASES
353514  |  LILRA5  |  DISEASES
3816  |  KLK1  |  DISEASES
284110  |  GSDMA  |  DISEASES
956  |  ENTPD3  |  DISEASES
474  |  ATOH1  |  DISEASES
6356  |  CCL11  |  DISEASES
6037  |  RNASE3  |  DISEASES
116844  |  LRG1  |  DISEASES
3479  |  IGF1  |  DISEASES
5734  |  PTGER4  |  DISEASES
3603  |  IL16  |  DISEASES
3308  |  HSPA4  |  DISEASES
5968  |  REG1B  |  DISEASES
6869  |  TACR1  |  DISEASES
1673  |  DEFB4A  |  DISEASES
1673  |  DEFB4A  |  DISEASES
1493  |  CTLA4  |  DISEASES
5068  |  REG3A  |  DISEASES
10663  |  CXCR6  |  DISEASES
94103  |  ORMDL3  |  DISEASES
3596  |  IL13  |  DISEASES
1901  |  S1PR1  |  DISEASES
3627  |  CXCL10  |  DISEASES
3575  |  IL7R  |  DISEASES
2353  |  FOS  |  DISEASES
56246  |  MRAP  |  DISEASES
654483  |  BOLA2B  |  DISEASES
6373  |  CXCL11  |  DISEASES
27087  |  B3GAT1  |  DISEASES
140886  |  PABPC5  |  DISEASES
197259  |  MLKL  |  DISEASES
2147  |  F2  |  DISEASES
5897  |  RAG2  |  DISEASES
1540  |  CYLD  |  DISEASES
5340  |  PLG  |  DISEASES
171389  |  NLRP6  |  DISEASES
116535  |  MRGPRF  |  DISEASES
3265  |  HRAS  |  DISEASES
6868  |  ADAM17  |  DISEASES
947  |  CD34  |  DISEASES
3310  |  HSPA6  |  DISEASES
836  |  CASP3  |  DISEASES
6578  |  SLCO2A1  |  DISEASES
1521  |  CTSW  |  DISEASES
84971  |  ATG4D  |  DISEASES
5771  |  PTPN2  |  DISEASES
5319  |  PLA2G1B  |  DISEASES
7172  |  TPMT  |  DISEASES
201625  |  DNAH12  |  DISEASES
3952  |  LEP  |  DISEASES
54472  |  TOLLIP  |  DISEASES
30835  |  CD209  |  DISEASES
57217  |  TTC7A  |  DISEASES
144811  |  LACC1  |  DISEASES
9377  |  COX5A  |  DISEASES
2529  |  FUT7  |  DISEASES
89872  |  AQP10  |  DISEASES
260436  |  FDCSP  |  DISEASES
4684  |  NCAM1  |  DISEASES
8630  |  HSD17B6  |  DISEASES
54984  |  PINX1  |  DISEASES
3579  |  CXCR2  |  DISEASES
9120  |  SLC16A6  |  DISEASES
80381  |  CD276  |  DISEASES
9370  |  ADIPOQ  |  DISEASES
140596  |  DEFB104A  |  DISEASES
90933  |  TRIM41  |  DISEASES
23765  |  IL17RA  |  DISEASES
414325  |  DEFB103A  |  DISEASES
6863  |  TAC1  |  DISEASES
149233  |  IL23R  |  DISEASES
256815  |  C10orf67  |  DISEASES
503618  |  DEFB104B  |  DISEASES
3039  |  HBA1  |  DISEASES
246330  |  PELI3  |  DISEASES
4312  |  MMP1  |  DISEASES
153562  |  MARVELD2  |  DISEASES
55600  |  ITLN1  |  DISEASES
8408  |  ULK1  |  DISEASES
55894  |  DEFB103B  |  DISEASES
9235  |  IL32  |  DISEASES
4584  |  MUC3A  |  DISEASES
940  |  CD28  |  DISEASES
150962  |  PUS10  |  DISEASES
9622  |  KLK4  |  DISEASES
89849  |  ATG16L2  |  DISEASES
6097  |  RORC  |  DISEASES
4094  |  MAF  |  DISEASES
146722  |  CD300LF  |  DISEASES
4843  |  NOS2  |  DISEASES
1435  |  CSF1  |  DISEASES
3563  |  IL3RA  |  DISEASES
10293  |  TRAIP  |  DISEASES
8784  |  TNFRSF18  |  DISEASES
1668  |  DEFA3  |  DISEASES
23046  |  KIF21B  |  DISEASES
50616  |  IL22  |  DISEASES
8651  |  SOCS1  |  DISEASES
1670  |  DEFA5  |  DISEASES
8624  |  PSMG1  |  DISEASES
9121  |  SLC16A5  |  DISEASES
9021  |  SOCS3  |  DISEASES
54014  |  BRWD1  |  DISEASES
8519  |  IFITM1  |  DISEASES
7850  |  IL1R2  |  DISEASES
552900  |  BOLA2  |  DISEASES
2520  |  GAST  |  DISEASES
6401  |  SELE  |  DISEASES
942  |  CD86  |  DISEASES
124460  |  SNX20  |  DISEASES
4088  |  SMAD3  |  DISEASES
3916  |  LAMP1  |  DISEASES
682  |  BSG  |  DISEASES
51363  |  CHST15  |  DISEASES
2152  |  F3  |  DISEASES
57178  |  ZMIZ1  |  DISEASES
51738  |  GHRL  |  DISEASES
124626  |  ZPBP2  |  DISEASES
8856  |  NR1I2  |  DISEASES
9075  |  CLDN2  |  DISEASES
1103  |  CHAT  |  DISEASES
114548  |  NLRP3  |  DISEASES
55795  |  PCID2  |  DISEASES
112744  |  IL17F  |  DISEASES
1576  |  CYP3A4  |  DISEASES
89781  |  HPS4  |  DISEASES
23583  |  SMUG1  |  DISEASES
3266  |  ERAS  |  DISEASES
2309  |  FOXO3  |  DISEASES
85480  |  TSLP  |  DISEASES
3329  |  HSPD1  |  DISEASES
7100  |  TLR5  |  DISEASES
6776  |  STAT5A  |  DISEASES
84639  |  IL1F10  |  DISEASES
3804  |  KIR2DL3  |  DISEASES
1364  |  CLDN4  |  DISEASES
400935  |  IL17REL  |  DISEASES
921  |  CD5  |  DISEASES
159296  |  NKX2-3  |  DISEASES
29949  |  IL19  |  DISEASES
3716  |  JAK1  |  DISEASES
9474  |  ATG5  |  DISEASES
3836  |  KPNA1  |  DISEASES
3605  |  IL17A  |  DISEASES
7332  |  UBE2L3  |  DISEASES
1499  |  CTNNB1  |  DISEASES
199953  |  TMEM201  |  DISEASES
729967  |  MORN2  |  DISEASES
1861  |  TOR1A  |  DISEASES
114770  |  PGLYRP2  |  DISEASES
9863  |  MAGI2  |  DISEASES
10533  |  ATG7  |  DISEASES
65251  |  ZNF649  |  DISEASES
100506658  |  OCLN  |  DISEASES
79710  |  MORC4  |  DISEASES
331  |  XIAP  |  DISEASES
355  |  FAS  |  DISEASES
4698  |  NDUFA5  |  DISEASES
5265  |  SERPINA1  |  DISEASES
3240  |  HP  |  DISEASES
3841  |  KPNA5  |  DISEASES
3476  |  IGBP1  |  DISEASES
5284  |  PIGR  |  DISEASES
6288  |  SAA1  |  DISEASES
1822  |  ATN1  |  DISEASES
64116  |  SLC39A8  |  DISEASES
283234  |  CCDC88B  |  DISEASES
10124  |  ARL4A  |  DISEASES
3683  |  ITGAL  |  DISEASES
5725  |  PTBP1  |  DISEASES
987  |  LRBA  |  DISEASES
4745  |  NELL1  |  DISEASES
3663  |  IRF5  |  DISEASES
10807  |  SDCCAG3  |  DISEASES
5802  |  PTPRS  |  DISEASES
60  |  ACTB  |  DISEASES
10803  |  CCR9  |  DISEASES
1524  |  CX3CR1  |  DISEASES
6775  |  STAT4  |  DISEASES
841  |  CASP8  |  DISEASES
2526  |  FUT4  |  DISEASES
6364  |  CCL20  |  DISEASES
6364  |  CCL20  |  DISEASES
9332  |  CD163  |  DISEASES
5602  |  MAPK10  |  DISEASES
57115  |  PGLYRP4  |  DISEASES
26191  |  PTPN22  |  DISEASES
387129  |  NPSR1  |  DISEASES
3123  |  HLA-DRB1  |  DISEASES
5697  |  PYY  |  DISEASES
7037  |  TFRC  |  DISEASES
4638  |  MYLK  |  DISEASES
55876  |  GSDMB  |  DISEASES
3135  |  HLA-G  |  DISEASES
5599  |  MAPK8  |  DISEASES
54106  |  TLR9  |  DISEASES
2530  |  FUT8  |  DISEASES
58484  |  NLRC4  |  DISEASES
2673  |  GFPT1  |  DISEASES
6772  |  STAT1  |  DISEASES
22904  |  SBNO2  |  DISEASES
9181  |  ARHGEF2  |  DISEASES
4283  |  CXCL9  |  DISEASES
7096  |  TLR1  |  DISEASES
7052  |  TGM2  |  DISEASES
7042  |  TGFB2  |  DISEASES
6580  |  SLC22A1  |  DISEASES
25936  |  NSL1  |  DISEASES
117289  |  TAGAP  |  DISEASES
92703  |  TMEM183A  |  DISEASES
7432  |  VIP  |  DISEASES
55765  |  C1orf106  |  DISEASES
5788  |  PTPRC  |  DISEASES
5743  |  PTGS2  |  DISEASES
4688  |  NCF2  |  DISEASES
58527  |  ABRACL  |  DISEASES
462  |  SERPINC1  |  DISEASES
356  |  FASLG  |  DISEASES
2214  |  FCGR3A  |  DISEASES
1490  |  CTGF  |  DISEASES
910  |  CD1B  |  DISEASES
911  |  CD1C  |  DISEASES
115352  |  FCRL3  |  DISEASES
632  |  BGLAP  |  DISEASES
3570  |  IL6R  |  DISEASES
7170  |  TPM3  |  DISEASES
441168  |  FAM26F  |  DISEASES
256536  |  TCERG1L  |  DISEASES
6283  |  S100A12  |  DISEASES
6280  |  S100A9  |  DISEASES
4014  |  LOR  |  DISEASES
10758  |  TRAF3IP2  |  DISEASES
262  |  AMD1  |  DISEASES
50624  |  CUZD1  |  DISEASES
1755  |  DMBT1  |  DISEASES
1893  |  ECM1  |  DISEASES
639  |  PRDM1  |  DISEASES
2209  |  FCGR1A  |  DISEASES
2209  |  FCGR1A  |  DISEASES
11085  |  ADAM30  |  DISEASES
58528  |  RRAGD  |  DISEASES
914  |  CD2  |  DISEASES
8517  |  IKBKG  |  DISEASES
3738  |  KCNA3  |  DISEASES
8771  |  TNFRSF6B  |  DISEASES
84795  |  PYROXD2  |  DISEASES
959  |  CD40LG  |  DISEASES
112817  |  HOGA1  |  DISEASES
84251  |  SGIP1  |  DISEASES
55225  |  RAVER2  |  DISEASES
5236  |  PGM1  |  DISEASES
1791  |  DNTT  |  DISEASES
953  |  ENTPD1  |  DISEASES
3725  |  JUN  |  DISEASES
64170  |  CARD9  |  DISEASES
7422  |  VEGFA  |  DISEASES
115201  |  ATG4A  |  DISEASES
958  |  CD40  |  DISEASES
4318  |  MMP9  |  DISEASES
9231  |  DLG5  |  DISEASES
9231  |  DLG5  |  DISEASES
2491  |  CENPI  |  DISEASES
27035  |  NOX1  |  DISEASES
9436  |  NCR2  |  DISEASES
6865  |  TACR2  |  DISEASES
2833  |  CXCR3  |  DISEASES
54952  |  TRNAU1AP  |  DISEASES
4153  |  MBL2  |  DISEASES
7099  |  TLR4  |  DISEASES
9966  |  TNFSF15  |  DISEASES
143162  |  FRMPD2  |  DISEASES
219771  |  CCNY  |  DISEASES
56288  |  PARD3  |  DISEASES
5535  |  PPP3R2  |  DISEASES
3118  |  HLA-DQA2  |  DISEASES
5320  |  PLA2G2A  |  DISEASES
30814  |  PLA2G2E  |  DISEASES
23252  |  OTUD3  |  DISEASES
54546  |  RNF186  |  DISEASES
23569  |  PADI4  |  DISEASES
3055  |  HCK  |  DISEASES
4795  |  NFKBIL1  |  DISEASES
50943  |  FOXP3  |  DISEASES
100507436  |  MICA  |  DISEASES
100507436  |  MICA  |  DISEASES
3107  |  HLA-C  |  DISEASES
7133  |  TNFRSF1B  |  DISEASES
6564  |  SLC15A1  |  DISEASES
4524  |  MTHFR  |  DISEASES
11074  |  TRIM31  |  DISEASES
3105  |  HLA-A  |  DISEASES
7056  |  THBD  |  DISEASES
81696  |  OR5V1  |  DISEASES
23130  |  ATG2A  |  DISEASES
51160  |  VPS28  |  DISEASES
8718  |  TNFRSF25  |  DISEASES
6520  |  SLC3A2  |  DISEASES
100505591  |  LRRC3C  |  DISEASES
51131  |  PHF11  |  DISEASES
414062  |  CCL3L3  |  DISEASES
9445  |  ITM2B  |  DISEASES
1536  |  CYBB  |  DISEASES
1114  |  CHGB  |  DISEASES
9308  |  CD83  |  DISEASES
2625  |  GATA3  |  DISEASES
11193  |  WBP4  |  DISEASES
387755  |  INSC  |  DISEASES
23586  |  DDX58  |  DISEASES
3559  |  IL2RA  |  DISEASES
3704  |  ITPA  |  DISEASES
3456  |  IFNB1  |  DISEASES
9960  |  USP3  |  DISEASES
56265  |  CPXM1  |  DISEASES
51284  |  TLR7  |  DISEASES
25849  |  PARM1  |  DISEASES
3662  |  IRF4  |  DISEASES
1045  |  CDX2  |  DISEASES
3486  |  IGFBP3  |  DISEASES
2813  |  GP2  |  DISEASES
90865  |  IL33  |  DISEASES
3717  |  JAK2  |  DISEASES
10333  |  TLR6  |  DISEASES
255189  |  PLA2G4F  |  DISEASES
50506  |  DUOX2  |  DISEASES
2877  |  GPX2  |  DISEASES
116534  |  MRGPRE  |  DISEASES
6370  |  CCL25  |  DISEASES
2524  |  FUT2  |  DISEASES
22900  |  CARD8  |  DISEASES
11009  |  IL24  |  DISEASES
55054  |  ATG16L1  |  DISEASES
55054  |  ATG16L1  |  DISEASES
4216  |  MAP3K4  |  DISEASES
65057  |  ACD  |  DISEASES
56954  |  NIT2  |  DISEASES
55773  |  TBC1D23  |  DISEASES
84299  |  MIEN1  |  DISEASES
6355  |  CCL8  |  DISEASES
6696  |  SPP1  |  DISEASES
1365  |  CLDN3  |  DISEASES
3122  |  HLA-DRA  |  DISEASES
2919  |  CXCL1  |  DISEASES
6387  |  CXCL12  |  DISEASES
3174  |  HNF4G  |  DISEASES
3676  |  ITGA4  |  DISEASES
4689  |  NCF4  |  DISEASES
4650  |  MYO9B  |  DISEASES
594857  |  NPS  |  DISEASES
3119  |  HLA-DQB1  |  DISEASES
123745  |  PLA2G4E  |  DISEASES
7442  |  TRPV1  |  DISEASES
3803  |  KIR2DL2  |  DISEASES
1439  |  CSF2RB  |  DISEASES
5970  |  RELA  |  DISEASES
23308  |  ICOSLG  |  DISEASES
221938  |  MMD2  |  DISEASES
63027  |  SLC22A23  |  DISEASES
7018  |  TF  |  DISEASES
152789  |  JAKMIP1  |  DISEASES
9873  |  FCHSD2  |  DISEASES
22891  |  ZNF365  |  DISEASES
23274  |  CLEC16A  |  DISEASES
9354  |  UBE4A  |  DISEASES
2641  |  GCG  |  DISEASES
3384  |  ICAM2  |  DISEASES
4295  |  MLN  |  DISEASES
4295  |  MLN  |  DISEASES
10551  |  AGR2  |  DISEASES
3718  |  JAK3  |  DISEASES
23005  |  MAPKBP1  |  DISEASES
388552  |  BLOC1S3  |  DISEASES
8399  |  PLA2G10  |  DISEASES
1438  |  CSF2RA  |  DISEASES
283463  |  MUC19  |  DISEASES
100137049  |  PLA2G4B  |  DISEASES
10107  |  TRIM10  |  DISEASES
91975  |  ZNF300  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
7124  |  TNF  |  DISEASES
3106  |  HLA-B  |  DISEASES
64167  |  ERAP2  |  DISEASES
4615  |  MYD88  |  DISEASES
27151  |  CPAMD8  |  DISEASES
3594  |  IL12RB1  |  DISEASES
4049  |  LTA  |  DISEASES
25822  |  DNAJB5  |  DISEASES
388372  |  CCL4L1  |  DISEASES
4588  |  MUC6  |  DISEASES
2876  |  GPX1  |  DISEASES
160857  |  CCDC122  |  DISEASES
6349  |  CCL3L1  |  DISEASES
1154  |  CISH  |  DISEASES
204801  |  NLRP11  |  DISEASES
834  |  CASP1  |  DISEASES
4050  |  LTB  |  DISEASES
3586  |  IL10  |  DISEASES
58155  |  PTBP2  |  DISEASES
3441  |  IFNA4  |  DISEASES
4485  |  MST1  |  DISEASES
4583  |  MUC2  |  DISEASES
55230  |  USP40  |  DISEASES
2859  |  GPR35  |  DISEASES
721  |  C4B  |  DISEASES
10201  |  NME6  |  DISEASES
138065  |  RNF183  |  DISEASES
4585  |  MUC4  |  DISEASES
111  |  ADCY5  |  DISEASES
56244  |  BTNL2  |  DISEASES
7511  |  XPNPEP1  |  DISEASES
2638  |  GC  |  DISEASES
51428  |  DDX41  |  DISEASES
8635  |  RNASET2  |  DISEASES
51079  |  NDUFA13  |  DISEASES
100289462  |  DEFB4B  |  DISEASES
9140  |  ATG12  |  DISEASES
2920  |  CXCL2  |  DISEASES
345611  |  IRGM  |  DISEASES
151306  |  GPBAR1  |  DISEASES
3620  |  IDO1  |  DISEASES
7033  |  TFF3  |  DISEASES
59351  |  PBOV1  |  DISEASES
10978  |  CLP1  |  DISEASES
4586  |  MUC5AC  |  DISEASES
727897  |  MUC5B  |  DISEASES
930  |  CD19  |  DISEASES
1232  |  CCR3  |  DISEASES
3684  |  ITGAM  |  DISEASES
11331  |  PHB2  |  DISEASES
5027  |  P2RX7  |  DISEASES
339145  |  FAM92B  |  DISEASES
169355  |  IDO2  |  DISEASES
7421  |  VDR  |  DISEASES
7421  |  VDR  |  DISEASES
8972  |  MGAM  |  DISEASES
317  |  APAF1  |  DISEASES
317  |  APAF1  |  DISEASES
567  |  B2M  |  DISEASES
820  |  CAMP  |  DISEASES
22861  |  NLRP1  |  DISEASES
100287879  |  LINC00994  |  DISEASES
348120  |  LINC01193  |  DISEASES
404663  |  LINC01194  |  DISEASES
404744  |  NPSR1-AS1  |  DISEASES
641373  |  NRON  |  DISEASES
677768  |  SCARNA13  |  DISEASES
619383  |  SCARNA9  |  DISEASES
27099  |  SND1-IT1  |  DISEASES
26810  |  SNORD41  |  DISEASES
26796  |  SNORD53  |  DISEASES
652995  |  UCA1  |  DISEASES
Locus(Waiting for update.)
Disease ID 39
Disease crohn disease
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:179)
HP:0010447  |  Fistula in ano  |  43
HP:0002583  |  Colitis  |  22
HP:0002664  |  Neoplasia  |  14
HP:0100279  |  Ulcerative colitis  |  13
HP:0002665  |  Lymphoma  |  10
HP:0002633  |  Vasculitis  |  9
HP:0005214  |  Bowel obstruction  |  9
HP:0030731  |  Carcinoma  |  8
HP:0000999  |  Pyoderma  |  7
HP:0001903  |  Anemia  |  7
HP:0002014  |  Diarrhea  |  6
HP:0001369  |  Arthritis  |  6
HP:0000143  |  Rectovaginal fistula  |  6
HP:0004320  |  Vaginal fistula  |  6
HP:0003765  |  Psoriasis  |  6
HP:0011034  |  Amyloid disease  |  6
HP:0002239  |  Gastrointestinal hemorrhage  |  5
HP:0002584  |  Intestinal hemorrhage  |  5
HP:0002955  |  Granulomatosis  |  5
HP:0030151  |  Cholangitis  |  5
HP:0012531  |  Pain  |  5
HP:0001733  |  Pancreatic inflammation  |  4
HP:0001735  |  Acute pancreatitis  |  4
HP:0012115  |  Liver inflammation  |  4
HP:0012089  |  Arteritis  |  4
HP:0012189  |  Hodgkin disease  |  4
HP:0000112  |  Nephropathy  |  4
HP:0002754  |  Bone infection  |  4
HP:0001909  |  Leukemia  |  4
HP:0000716  |  Depression  |  3
HP:0001045  |  Blotchy loss of skin color  |  3
HP:0001945  |  Fever  |  3
HP:0001513  |  Obesity  |  3
HP:0001370  |  Rheumatoid arthritis  |  3
HP:0004871  |  Perineal fistula  |  3
HP:0100507  |  Folate deficiency  |  3
HP:0012452  |  Restless legs  |  3
HP:0002595  |  Gastrointestinal atony  |  3
HP:0002725  |  Systemic lupus erythematosus  |  3
HP:0012378  |  Fatigue  |  3
HP:0001297  |  Cerebral vascular events  |  3
HP:0002090  |  Pneumonia  |  3
HP:0100523  |  Hepatic abscess  |  3
HP:0000939  |  Osteoporosis  |  3
HP:0002352  |  Leukoencephalopathy  |  3
HP:0002721  |  Immunodeficiency  |  3
HP:0000969  |  Dropsy  |  3
HP:0100512  |  Vitamin D deficiency  |  2
HP:0012324  |  Myeloid leukemia  |  2
HP:0005681  |  Juvenile idiopathic arthritis  |  2
HP:0000100  |  Nephrosis  |  2
HP:0100653  |  Optic neuritis  |  2
HP:0004398  |  Peptic ulcer  |  2
HP:0003003  |  Colon cancer  |  2
HP:0000739  |  Anxiety  |  2
HP:0100614  |  Muscle inflammation  |  2
HP:0001287  |  Meningitis  |  2
HP:0001081  |  Gallstones  |  2
HP:0004808  |  Acute myelogenous leukemia  |  2
HP:0002140  |  Ischemic stroke  |  2
HP:0002024  |  Intestinal malabsorption  |  2
HP:0002586  |  Peritonitis  |  2
HP:0001824  |  Weight loss  |  2
HP:0001876  |  Low blood cell count  |  2
HP:0012190  |  T cell lymphoma  |  2
HP:0012219  |  Erythema nodosum  |  2
HP:0004395  |  Malnutrition  |  2
HP:0040154  |  Hidradenitis suppurativa  |  2
HP:0012390  |  Anal fissure  |  2
HP:0002573  |  Bloody diarrhea  |  2
HP:0002242  |  Enteropathy  |  2
HP:0005263  |  Gastritis  |  2
HP:0002027  |  Abdominal pain  |  2
HP:0002576  |  Intussusception  |  2
HP:0000491  |  Corneal inflammation  |  2
HP:0004936  |  Blood clot in vein  |  2
HP:0000853  |  Goitre  |  2
HP:0002608  |  Celiac disease  |  2
HP:0001873  |  Low platelet count  |  2
HP:0001402  |  Hepatocellular carcinoma  |  2
HP:0010783  |  Erythema  |  2
HP:0001004  |  Lymphatic obstruction  |  1
HP:0002840  |  Lymphadenitis  |  1
HP:0000093  |  Proteinuria  |  1
HP:0002013  |  Emesis  |  1
HP:0002890  |  Thyroid carcinoma  |  1
HP:0000579  |  Nasolacrimal duct obstruction  |  1
HP:0000938  |  Decreased bone mineral density  |  1
HP:0000704  |  Pyorrhea  |  1
HP:0001907  |  Thromboembolic disease  |  1
HP:0000787  |  Renal calculi  |  1
HP:0000508  |  Drooping upper eyelid  |  1
HP:0002566  |  Intestinal malrotation  |  1
HP:0100607  |  Painful menstruation  |  1
HP:0000010  |  Frequent urinary tract infections  |  1
HP:0000855  |  Insulin resistance  |  1
HP:0001395  |  Hepatic fibrosis  |  1
HP:0000099  |  Glomerular nephritis  |  1
HP:0012735  |  Coughing  |  1
HP:0001510  |  Growth deficiency  |  1
HP:0012714  |  Severe hearing loss  |  1
HP:0100825  |  Inflammation of the lips  |  1
HP:0001678  |  Atrioventricular block  |  1
HP:0007302  |  Bipolar disorder  |  1
HP:0005318  |  Cerebral vasculitis  |  1
HP:0002113  |  Pulmonary infiltrates  |  1
HP:0000123  |  Nephritis  |  1
HP:0001919  |  Acute renal failure  |  1
HP:0000720  |  Mood swings  |  1
HP:0200029  |  Cutaneous vasculitis  |  1
HP:0100764  |  Lymphangioma  |  1
HP:0001548  |  Overgrowth  |  1
HP:0012851  |  Narrowing of the colon  |  1
HP:0001888  |  Lymphocytopenia  |  1
HP:0002039  |  Anorexia  |  1
HP:0011505  |  Cystoid macular edema  |  1
HP:0002613  |  Biliary cirrhosis  |  1
HP:0002861  |  Melanoma  |  1
HP:0000365  |  Hearing impairment  |  1
HP:0001394  |  Hepatic cirrhosis  |  1
HP:0002917  |  Low blood magnesium levels  |  1
HP:0005901  |  Chronic recurrent multifocal osteomyelitis  |  1
HP:0009830  |  Peripheral neuritis  |  1
HP:0001056  |  Milia  |  1
HP:0100584  |  Endocarditis  |  1
HP:0012223  |  Ruptured spleen  |  1
HP:0001660  |  Common arterial trunk  |  1
HP:0002251  |  Hirschsprung megacolon  |  1
HP:0100665  |  Angiooedema  |  1
HP:0001061  |  Acne  |  1
HP:0001138  |  Damaged optic nerve  |  1
HP:0002018  |  Nausea  |  1
HP:0100590  |  Rectal fistula  |  1
HP:0200123  |  Chronic liver inflammation  |  1
HP:0003419  |  Low back pain  |  1
HP:0001970  |  Interstitial nephritis  |  1
HP:0002500  |  Leukoaraiosis  |  1
HP:0001890  |  Autoimmune hemolytic anemia  |  1
HP:0005211  |  Midgut malrotation  |  1
HP:0002910  |  Elevated transaminases  |  1
HP:0010280  |  Stomatitis  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0012538  |  Gluten sensitivity  |  1
HP:0004349  |  Reduced bone mineral density  |  1
HP:0002019  |  Dyschezia  |  1
HP:0002133  |  Status epilepticus  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0003095  |  Septic arthritis  |  1
HP:0100758  |  Gangrene  |  1
HP:0005224  |  Rectal abscess  |  1
HP:0002593  |  Intestinal lymphangiectasia  |  1
HP:0000498  |  Inflammation of eyelids  |  1
HP:0100796  |  Orchitis  |  1
HP:0001009  |  Telangiectases  |  1
HP:0000979  |  Purpura  |  1
HP:0004387  |  Enterocolitis  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0002749  |  Osteomalacia  |  1
HP:0003613  |  Antiphospholipid antibodies  |  1
HP:0003418  |  Back pain  |  1
HP:0001878  |  Haemolytic anaemia  |  1
HP:0001820  |  Leukonychia  |  1
HP:0100532  |  Scleritis  |  1
HP:0004322  |  Stature below 3rd percentile  |  1
HP:0012034  |  Liposarcoma  |  1
HP:0000488  |  Noninflammatory retina disease  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0010628  |  Facial palsy, unilateral or bilateral  |  1
HP:0002895  |  Papillary thyroid carcinoma  |  1
HP:0200039  |  Pustules  |  1
HP:0002578  |  Gastroparesis  |  1
HP:0005521  |  Disseminated intravascular coagulation  |  1
HP:0003712  |  Hypertrophic muscles  |  1
HP:0002028  |  Chronic diarrhea  |  1
HP:0100819  |  Intestinal fistula  |  1
HP:0007606  |  Multiple cutaneous malignancies  |  1
HP:0005305  |  Cerebral vein thrombosis  |  1
HP:0002204  |  Pulmonary embolism  |  1
HP:0001289  |  Confusion  |  1
Disease ID 39
Disease crohn disease
Manually Symptom
UMLS  | Name(Total Manually Symptoms:84)
C2707258  |  infections
C2697310  |  sarcoidosis
C2678504  |  osteoporosis
C2364133  |  infection
C2318511  |  nonalcoholic steatohepatitis
C2046121  |  aortic dissection
C1963274  |  vasculitis
C1963198  |  pancreatitis
C1963184  |  nystagmus
C1963091  |  diarrhea
C1562901  |  peripheral ulcerative keratitis
C1550639  |  fistula
C1000483  |  anemia
C0949690  |  spondylarthritis
C0949022  |  rectal cancer
C0749914  |  urethrocutaneous fistula
C0748159  |  pulmonary involvement
C0699791  |  gastric carcinoma
C0582430  |  adenocarcinoma of the ileum
C0566602  |  primary sclerosing cholangitis
C0547058  |  pseudopolyposis
C0409207  |  arthritis of the hip
C0346627  |  intestinal cancer
C0279637  |  anal carcinoma
C0278803  |  small bowel adenocarcinoma
C0278803  |  adenocarcinoma of the small intestine
C0272404  |  hyposplenism
C0267532  |  diversion colitis
C0267465  |  intestinal stricture
C0267373  |  intestinal bleeding
C0243001  |  intra-abdominal abscesses
C0243001  |  intra-abdominal abscess
C0238419  |  fournier gangrene
C0238196  |  carcinoma of the small intestine
C0238196  |  carcinoma of the small bowel
C0238051  |  cerebral vasculitis
C0235950  |  zinc deficiency
C0235329  |  small bowel obstruction
C0221166  |  paraparesis
C0175702  |  williams syndrome
C0162429  |  malnutrition
C0162323  |  polyarthritis
C0156272  |  vesico-intestinal fistula
C0156272  |  enterovesical fistula
C0152026  |  retinal vasculitis
C0086981  |  sicca
C0085652  |  pyoderma gangrenosum
C0085077  |  sweet syndrome
C0040038  |  thromboembolism
C0039263  |  takayasu disease
C0038833  |  superior vena cava syndrome
C0038450  |  stridor
C0037293  |  skin tags
C0037198  |  intracranial sinus thrombosis
C0035067  |  renal artery stenosis
C0034895  |  rectovaginal fistulas
C0034212  |  pyoderma
C0033860  |  psoriasis
C0033845  |  pseudotumor cerebri
C0032568  |  pseudopolyp
C0032285  |  pneumoniae
C0030246  |  palmoplantar pustulosis
C0029166  |  oral manifestations
C0029166  |  oral manifestation
C0027720  |  nephrosis
C0027033  |  intestinal myiasis
C0025037  |  meckel diverticulum
C0024299  |  lymphoma
C0022951  |  lactose malabsorption
C0022408  |  arthropathy
C0022408  |  arthropathies
C0021933  |  intussusception
C0021833  |  intestinal fistula
C0020295  |  hydronephrosis
C0019080  |  hemorrhage
C0017661  |  iga nephropathy
C0017536  |  giardiasis
C0017181  |  gastrointestinal hemorrhage
C0014743  |  erythema nodosum
C0009402  |  colorectal carcinomas
C0007102  |  colonic cancer
C0006413  |  burkitt's lymphoma
C0003504  |  aortic valve insufficiency
C0001339  |  acute pancreatitis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:166)
C0016169  |  fistula  |  44
C0021831  |  bowel disease  |  25
C0009319  |  colitis  |  18
C0009450  |  infection  |  15
C0009324  |  ulcerative colitis  |  12
C0000833  |  abscess  |  11
C0030524  |  paratuberculosis  |  9
C0024299  |  lymphoma  |  9
C0042384  |  vasculitis  |  8
C0009814  |  stenosis  |  7
C0278803  |  small bowel adenocarcinoma  |  7
C0002871  |  anemia  |  7
C0033860  |  psoriasis  |  6
C0042253  |  vaginal fistula  |  6
C0040053  |  thrombosis  |  6
C0566602  |  primary sclerosing cholangitis  |  6
C0008313  |  sclerosing cholangitis  |  6
C0001418  |  adenocarcinoma  |  6
C0003864  |  arthritis  |  5
C0011991  |  diarrhea  |  5
C0002726  |  amyloidosis  |  5
C0021390  |  inflammatory bowel diseases  |  5
C0521173  |  granulomatosis  |  5
C0085652  |  pyoderma gangrenosum  |  5
C0267373  |  intestinal bleeding  |  5
C0243001  |  intra-abdominal abscess  |  5
C0030193  |  pain  |  4
C0030305  |  pancreatitis  |  4
C0001339  |  acute pancreatitis  |  4
C0039263  |  takayasu's arteritis  |  4
C0009402  |  colorectal cancer  |  4
C0029443  |  osteomyelitis  |  4
C0019158  |  hepatitis  |  4
C0034895  |  rectovaginal fistula  |  4
C0007113  |  rectal cancer  |  4
C0028754  |  obesity  |  3
C0346627  |  intestinal cancer  |  3
C0018202  |  granulomatous vasculitis  |  3
C0024141  |  systemic lupus erythematosus  |  3
C0021843  |  intestinal obstruction  |  3
C0267000  |  pyostomatitis vegetans  |  3
C0029456  |  osteoporosis  |  3
C0015967  |  fever  |  3
C0409974  |  lupus erythematosus  |  3
C0032285  |  pneumonia  |  3
C0036202  |  sarcoidosis  |  3
C0267466  |  colonic stricture  |  3
C0021845  |  bowel perforation  |  3
C0399496  |  orofacial granulomatosis  |  3
C0016412  |  folate deficiency  |  3
C1609502  |  portal venous gas  |  3
C0015672  |  fatigue  |  3
C0021843  |  bowel obstruction  |  3
C0023524  |  progressive multifocal leukoencephalopathy  |  3
C0268380  |  systemic amyloidosis  |  3
C0023885  |  liver abscess  |  3
C0267358  |  duodenal fistula  |  3
C0021079  |  immunosuppression  |  2
C0042487  |  venous thrombosis  |  2
C0949691  |  spondyloarthropathy  |  2
C0025289  |  meningitis  |  2
C0021933  |  intussusception  |  2
C0019829  |  hodgkin's lymphoma  |  2
C1994997  |  intestinal symptoms  |  2
C0162429  |  malnutrition  |  2
C0030920  |  peptic ulcer  |  2
C0008350  |  gallstones  |  2
C0156156  |  gallstone ileus  |  2
C0221014  |  secondary amyloidosis  |  2
C0024523  |  malabsorption  |  2
C0451641  |  urolithiasis  |  2
C0426576  |  gastrointestinal symptoms  |  2
C0016167  |  anal fissure  |  2
C2350476  |  orbital myositis  |  2
C0027726  |  nephrotic syndrome  |  2
C0162836  |  hidradenitis suppurativa  |  2
C0018188  |  granuloma  |  2
C0007570  |  celiac disease  |  2
C0000737  |  abdominal pain  |  2
C0030312  |  pancytopenia  |  2
C0007102  |  colon cancer  |  2
C0027121  |  myositis  |  2
C1275022  |  parastomal pyoderma gangrenosum  |  2
C0023467  |  acute myeloid leukemia  |  2
C0153425  |  small bowel cancer  |  2
C0030785  |  pelvic abscess  |  2
C0243001  |  abdominal abscess  |  2
C0019204  |  hepatocellular carcinoma  |  2
C0034895  |  rectovaginal fistulas  |  2
C0037284  |  skin lesions  |  2
C0238196  |  carcinoma of the small bowel  |  2
C0346627  |  bowel cancer  |  2
C0948008  |  ischemic stroke  |  2
C0235329  |  small bowel obstruction  |  2
C0040034  |  thrombocytopenia  |  2
C0014743  |  erythema nodosum  |  2
C0017152  |  gastritis  |  2
C0267830  |  pyogenic liver abscess  |  1
C0238196  |  small bowel carcinoma  |  1
C0039263  |  takayasu disease  |  1
C0016171  |  intestinal fistula  |  1
C0349533  |  intestinal lymphoma  |  1
C0042769  |  virus infection  |  1
C0003509  |  aortitis  |  1
C0156272  |  enterovesical fistula  |  1
C0410422  |  chronic recurrent multifocal osteomyelitis  |  1
C0263210  |  pyoderma faciale  |  1
C0011570  |  depression  |  1
C0267467  |  colonic intussusception  |  1
C0037285  |  skin manifestations  |  1
C0748159  |  pulmonary involvement  |  1
C0243001  |  intra-abdominal abscesses  |  1
C1333984  |  hepatosplenic t-cell lymphoma  |  1
C0037274  |  dermatoses  |  1
C0009402  |  colorectal carcinoma  |  1
C0023895  |  liver disease  |  1
C0243001  |  abdominal abscesses  |  1
C0041331  |  splenic tuberculosis  |  1
C0024299  |  lymphomas  |  1
C0028709  |  nutritional problems  |  1
C0085584  |  encephalopathy  |  1
C0267465  |  intestinal stricture  |  1
C0017086  |  gangrene  |  1
C0025037  |  meckel's diverticulum  |  1
C0085077  |  sweet syndrome  |  1
C0235896  |  pulmonary infiltrate  |  1
C0025162  |  toxic megacolon  |  1
C0856169  |  endothelial dysfunction  |  1
C0279637  |  carcinoma of the anus  |  1
C0162316  |  iron deficiency  |  1
C0334108  |  polyposis  |  1
C0024312  |  lymphopenia  |  1
C0002880  |  autoimmune hemolytic anemia  |  1
C0012817  |  diverticulum  |  1
C0040038  |  thromboembolism  |  1
C0010823  |  cmv infection  |  1
C0278803  |  adenocarcinoma of the small bowel  |  1
C0272404  |  hyposplenism  |  1
C0600268  |  granulomatous cheilitis  |  1
C0085077  |  sweet's syndrome  |  1
C0155305  |  ischemic optic neuropathy  |  1
C0032568  |  pseudopolyposis  |  1
C0040053  |  thrombus  |  1
C0031117  |  peripheral neuropathy  |  1
C0005944  |  metabolic bone disease  |  1
C0333039  |  phytobezoar  |  1
C0042870  |  vitamin d deficiency  |  1
C0014118  |  endocarditis  |  1
C0004030  |  aspergillosis  |  1
C0003123  |  anorexia  |  1
C0001418  |  adenocarcinomas  |  1
C0392525  |  nephrolithiasis  |  1
C0267760  |  mesenteric abscess  |  1
C0029134  |  optic neuritis  |  1
C0267465  |  intestinal stenosis  |  1
C0025309  |  meningoencephalitis  |  1
C0014356  |  enterocolitis  |  1
C0008312  |  primary biliary cirrhosis  |  1
C0043092  |  wegener's granulomatosis  |  1
C0005940  |  bone disease  |  1
C0010823  |  cytomegalovirus infection  |  1
C1332257  |  anal adenocarcinoma  |  1
C0598608  |  hyperhomocysteinemia  |  1
C0003874  |  septic arthritis  |  1
C1562901  |  peripheral ulcerative keratitis  |  1
C0002878  |  hemolytic anemia  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:836)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs100454312452226655054ATG16L1umls:C0010346BeFreeDetection of Mycobacterium avium subspecies paratuberculosis in patients with Crohn's disease is unrelated to the presence of single nucleotide polymorphisms rs2241880 (ATG16L1) and rs10045431 (IL12B).0.3678631532014NA5159387525AC
rs10045431185873943593IL12Bumls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1448320322008NA5159387525AC
rs10045431205709663593IL12Bumls:C0010346GAD[Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.]0.1448320322010NA5159387525AC
rs10045431245222663593IL12Bumls:C0010346BeFreeDetection of Mycobacterium avium subspecies paratuberculosis in patients with Crohn's disease is unrelated to the presence of single nucleotide polymorphisms rs2241880 (ATG16L1) and rs10045431 (IL12B).0.1448320322014NA5159387525AC
rs100481917786191149233IL23Rumls:C0010346BeFreers1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.0.3705974352007IL23R167204530GA
rs100481917804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167204530GA
rs10048192006673655054ATG16L1umls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.3678631532010IL23R167204530GA
rs100481920066736149233IL23Rumls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.3705974352010IL23R167204530GA
rs10048192006673664127NOD2umls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.562010IL23R167204530GA
rs10048192006673650941IBD5umls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.0496165762010IL23R167204530GA
rs100639492428444727034ACAD8umls:C0010346BeFreeA genetic variant (rs10063949-G) in the SLC23A1 ascorbate transporter locus was identified and is associated with an increased risk of CD in a white Canadian IBD cohort.0.0127577682014SLC23A15139383837TC
rs100651722424722355054ATG16L1umls:C0010346BeFreeWe found a genetic interaction between reference SNP (rs)2241880 (ATG16L1) and rs10065172 (IRGM) in CD.0.3678631532014IRGM5150848436CT
rs100656372312823379722ANKRD55umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012ANKRD55556143024CT
rs1018104221102463150962PUS10umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1273725382010PUS10260997124CT
rs1018104221102463150962PUS10umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1273725382010PUS10260997124CT
rs102103021755430055054ATG16L1umls:C0010346GWASCATGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.0.3678631532007ATG16L12233250193CT
rs10227521102463746TMEM258umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1223670322010TMEM2581161790331TC
rs10227521102463746TMEM258umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1223670322010TMEM2581161790331TC
rs1045642172603535243ABCB1umls:C0010346BeFreeA total of 211 patients with Crohn's disease (CD), 97 patients with ulcerative colitis (UC), and 212 control subjects were investigated for the presence of MDR1 G2677T/A and C3435T polymorphisms.0.0260036762007ABCB1787509329AT,G
rs1045642166330485243ABCB1umls:C0010346BeFreeThe present study examined the association of ABCB1 C3435T and G2677T/A in a large British case-control cohort of 828 Crohn's disease, 580 ulcerative colitis (UC) cases, and 285 healthy controls.0.0260036762006ABCB1787509329AT,G
rs1045642156855405243ABCB1umls:C0010346BeFreeThis was a case-control analysis of MDR1 C3435T and G2677T SNPs in a large well-characterized Scottish white cohort (335 with ulcerative colitis [UC], 268 with Crohn's disease [CD], and 370 healthy controls).0.0260036762005ABCB1787509329AT,G
rs10486483231282338935SKAP2umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012SKAP2;LOC105375204726852821GA
rs104959032110246363892THADAumls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1223670322010THADA243579779CT
rs104959032110246363892THADAumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1223670322010THADA243579779CT
rs1049793196700781610DAOumls:C0010346GAD[To analyse the possible influence of a non-synonymous single nucleotide polymorphism (SNP) of the histamine-degrading enzyme diamine oxidase (DAO) on genetic susceptibility to Crohn's disease (CD).]0.0023670322009AOC1;LOC1053755677150860577CG
rs10499563247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014NA722720869TC
rs10499563247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014NA722720869TC
rs10499563247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014NA722720869TC
rs10499563247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014NA722720869TC
rs10499563247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014NA722720869TC
rs10499563247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014NA722720869TC
rs104995632477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014NA722720869TC
rs10499563247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014NA722720869TC
rs10499563247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014NA722720869TC
rs10499563247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014NA722720869TC
rs104995632477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014NA722720869TC
rs10499563247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014NA722720869TC
rs1050152196601516583SLC22A4umls:C0010346BeFreeCarrying a functional single nucleotide polymorphism (L503F, c. 1672 C>T) in the gene for the Na-dependent organic cation transporter (OCTN1), increases the risk of Crohn's disease (CD) in some, but not all, populations.0.0796595422009SLC22A4;LOC5531035132340627CT
rs1050152222066296583SLC22A4umls:C0010346BeFreeThe human OCTN1 (SLC22A4) reconstituted in liposomes catalyzes acetylcholine transport which is defective in the mutant L503F associated to the Crohn's disease.0.0796595422012SLC22A4;LOC5531035132340627CT
rs1073410522412388256536TCERG1Lumls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.0023670322012NA10131373856GA
rs10758669220651123717JAK2umls:C0010346BeFreeThe JAK2 variant rs10758669 in Crohn's disease: altering the intestinal barrier as one mechanism of action.0.0140066952012NA94981602CA
rs10758669185873943717JAK2umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0140066952008NA94981602CA
rs10758669243852393717JAK2umls:C0010346BeFreeJAK2 rs10758669 polymorphisms and susceptibility to ulcerative colitis and Crohn's disease: a meta-analysis.0.0140066952015NA94981602CA
rs107586691858739410171RCL1umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0023670322008NA94981602CA
rs107616592110246322891ZNF365umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1373835492010NA1062685804AG
rs107616591755430022891ZNF365umls:C0010346GAD[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]0.1373835492007NA1062685804AG
rs1080104717554261339479BRINP3umls:C0010346GAD[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]0.0023670322007NA1191590226AT
rs1088336521514341159296NKX2-3umls:C0010346BeFreeA total of 344 patients with Crohn's disease (CD), 253 patients with ulcerative colitis (UC), and 243 healthy controls (HCs) were genotyped for 3 tag-single nucleotide polymorphisms (SNPs; rs10883365, rs888208, and rs11596008) around NKX2.3.0.2743860362011LINC014751099528007GA
rs10883365175542612805GOT1umls:C0010346GAD[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]0.0073725382007LINC014751099528007GA
rs10883365175543002805GOT1umls:C0010346GAD[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]0.0073725382007LINC014751099528007GA
rs1088336517554261101927324LINC01475umls:C0010346GWASCATSequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.0.122007LINC014751099528007GA
rs1088336517554300101927324LINC01475umls:C0010346GWASCATGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.0.122007LINC014751099528007GA
rs1088967617804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167256884CA
rs1088967717804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167259437CA
rs1094726123850713101929163LOC101929163umls:C0010346GWASCATGenome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.0.122014BTNL2;LOC101929163632405455GT
rs109472612385071356244BTNL2umls:C0010346GWASCATGenome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.0.1253628242014BTNL2;LOC101929163632405455GT
rs10975003218317333717JAK2umls:C0010346BeFreeExcept rs10975003 from the JAK2 locus, none showed positive association with Crohn's disease.0.0140066952011NA95213687TC
rs109952711858739422891ZNF365umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1373835492008NA1062678726GC
rs1117559318587394120892LRRK2umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0063627152008LOC1053697351240208138CT
rs1117559318587394283463MUC19umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1250055062008LOC1053697351240208138CT
rs1119014018587394101927324LINC01475umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.122008NKX2-3;LINC014751099531836TC
rs1119014018587394159296NKX2-3umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.2743860362008NKX2-3;LINC014751099531836TC
rs1119014122412388159296NKX2-3umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.2743860362012NKX2-3;LINC014751099532633CT
rs1119014122412388101927324LINC01475umls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.122012NKX2-3;LINC014751099532633CT
rs1119014122412388159296NKX2-3umls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.2743860362012NKX2-3;LINC014751099532633CT
rs1120900217804789400757C1orf141umls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.122007C1orf141167124778TC
rs1120900317804789400757C1orf141umls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.122007C1orf141167135449GT
rs11209026249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014IL23R167240275GA
rs112090262008248364127NOD2umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.562010IL23R167240275GA
rs112090262525951164127NOD2umls:C0010346BeFreeWe observed the association between Crohn's disease and NOD2 (rs17313265, 0.28 in CD, 0.19 in controls, OR 1.5, p = 9×10-6) and IL23R (rs11209026, 0.026 in CD, 0.0.071 in controls, OR 0.4, p = 3.8×10-4).0.562014IL23R167240275GA
rs1120902620192940149233IL23Rumls:C0010346GAD[Association of the interleukin-23 receptor gene variant rs11209026 with Crohn's disease in German children.]0.3705974352010IL23R167240275GA
rs11209026249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014IL23R167240275GA
rs1120902625259511149233IL23Rumls:C0010346BeFreeWe observed the association between Crohn's disease and NOD2 (rs17313265, 0.28 in CD, 0.19 in controls, OR 1.5, p = 9×10-6) and IL23R (rs11209026, 0.026 in CD, 0.0.071 in controls, OR 0.4, p = 3.8×10-4).0.3705974352014IL23R167240275GA
rs1120902617894849149233IL23Rumls:C0010346BeFreeIL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand Caucasians with inflammatory bowel disease.0.3705974352007IL23R167240275GA
rs112090262008248355054ATG16L1umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3678631532010IL23R167240275GA
rs1120902622293688149233IL23Rumls:C0010346GAD[One is SNP rs11209026 in exon 9 of IL23R for association with Crohn's disease, which is predicted to be probably damaging by PolyPhen2.]0.3705974352012IL23R167240275GA
rs1120902617447842149233IL23Rumls:C0010346GWASCATTwo of these (IL23R on Chromosome 1 and CARD15 on Chromosome 16) correspond to genes previously reported to be associated with CD.0.3705974352007IL23R167240275GA
rs11209026249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014IL23R167240275GA
rs1120902617877509149233IL23Rumls:C0010346BeFreeHeterozygosity for IL23R p.Arg381Gln confers a protective effect not only against Crohn's disease but also ulcerative colitis.0.3705974352007IL23R167240275GA
rs1120902622293688149233IL23Rumls:C0010346GWASCATOne is SNP rs11209026 in exon 9 of IL23R for association with Crohn's disease, which is predicted to be probably damaging by PolyPhen2.0.3705974352012IL23R167240275GA
rs112090261789484955054ATG16L1umls:C0010346BeFreeIL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand Caucasians with inflammatory bowel disease.0.3678631532007IL23R167240275GA
rs1120902617804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167240275GA
rs112090262497146126191PTPN22umls:C0010346BeFreeAfter Bonferroni correction for multiple testing, both the homozygous and the heterozygous variant genotypes of IL23R G>A(rs11209026) (OR(CD,adj): 0.38, 95% CI: 0.21-0.67, p = 0.03; OR(IBD,adj) 0.43, 95% CI: 0.28-0.67, p = 0.007) and PTPN22 1858 G>A(rs2476601) (OR(CD,unadj) 0.54, 95% CI: 0.41-0.72, p = 7*10-4; OR(IBD,unadj): 0.61, 95% CI: 0.48-0.77, p = 0.001) were associated with reduced risk of CD.0.1537572762014IL23R167240275GA
rs1120902624971461149233IL23Rumls:C0010346BeFreeAfter Bonferroni correction for multiple testing, both the homozygous and the heterozygous variant genotypes of IL23R G>A(rs11209026) (OR(CD,adj): 0.38, 95% CI: 0.21-0.67, p = 0.03; OR(IBD,adj) 0.43, 95% CI: 0.28-0.67, p = 0.007) and PTPN22 1858 G>A(rs2476601) (OR(CD,unadj) 0.54, 95% CI: 0.41-0.72, p = 7*10-4; OR(IBD,unadj): 0.61, 95% CI: 0.48-0.77, p = 0.001) were associated with reduced risk of CD.0.3705974352014IL23R167240275GA
rs1120902621102463149233IL23Rumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.3705974352010IL23R167240275GA
rs1120902618030204149233IL23Rumls:C0010346BeFreeEvaluation of the interleukin-23 receptor gene coding variant R381Q in pediatric and adult Crohn disease.0.3705974352007IL23R167240275GA
rs1120902620192940149233IL23Rumls:C0010346BeFreeAssociation of the interleukin-23 receptor gene variant rs11209026 with Crohn's disease in German children.0.3705974352010IL23R167240275GA
rs1120902620082483149233IL23Rumls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3705974352010IL23R167240275GA
rs1120902622936669149233IL23Rumls:C0010346GWASCATA genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.0.3705974352013IL23R167240275GA
rs1120902622412388149233IL23Rumls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.3705974352012IL23R167240275GA
rs1120902618383363149233IL23Rumls:C0010346BeFreeRecent studies have shown that a nonsynonymous single-nucleotide polymorphism (SNP) (Arg381Gln; rs11209026) in the interleukin-23 receptor (IL-23R) gene on chromosome 1p31 is associated with Crohn's disease and psoriasis.0.3705974352008IL23R167240275GA
rs1120902622293688149233IL23Rumls:C0010346BeFreeOne is SNP rs11209026 in exon 9 of IL23R for association with Crohn's disease, which is predicted to be probably damaging by PolyPhen2.0.3705974352012IL23R167240275GA
rs112290302241238829015SLC43A3umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.0023670322012NA1157435536CT
rs11422872110246310067SCAMP3umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1223670322010SCAMP31155260340CT
rs1146578819700857149233IL23Rumls:C0010346BeFreeContribution of rs11465788 in IL23R gene to Crohn's disease susceptibility and phenotype in Chinese population.0.3705974352009IL23R167182611CT
rs1146580217804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167219915AC,T
rs1146580417804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167236843TG
rs1146580418587394149233IL23Rumls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.3705974352008IL23R167236843TG
rs1146580420570966149233IL23Rumls:C0010346GWASCATFucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.0.3705974352010IL23R167236843TG
rs11465996247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014LY96873989727CG
rs11465996247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014LY96873989727CG
rs11465996247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014LY96873989727CG
rs11465996247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014LY96873989727CG
rs11465996247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014LY96873989727CG
rs11465996247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014LY96873989727CG
rs11465996247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014LY96873989727CG
rs11465996249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014LY96873989727CG
rs11465996247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014LY96873989727CG
rs114659962477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014LY96873989727CG
rs114659962477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014LY96873989727CG
rs11465996249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014LY96873989727CG
rs11465996247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014LY96873989727CG
rs11465996249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014LY96873989727CG
rs11465996247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014LY96873989727CG
rs1156425821102463283463MUC19umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1250055062010MUC19;LOC1053697361240398498GA
rs11574514224123885699PSMB10umls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.1226384742012PSMB101667937477CT
rs11574514224123885699PSMB10umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.1226384742012PSMB101667937477CT
rs1158438318587394647215MROH3Pumls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1223670322008MROH3P1200966738TC
rs1158438318587394647215MROH3Pumls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.1223670322008MROH3P1200966738TC
rs1159600821514341159296NKX2-3umls:C0010346BeFreeA total of 344 patients with Crohn's disease (CD), 253 patients with ulcerative colitis (UC), and 243 healthy controls (HCs) were genotyped for 3 tag-single nucleotide polymorphisms (SNPs; rs10883365, rs888208, and rs11596008) around NKX2.3.0.2743860362011LINC014751099527557CT
rs11676348260713993579CXCR2umls:C0010346BeFreeThe minor allele (T) in SNP rs11676348, located downstream from CXCR2 that has been implicated in CRC progression, is associated with a lower risk of CRC, particularly tumors with a mucinous component, Crohn's-like reaction and MSI-high.0.0002714422015NA2218145423CT
rs11742570211024631601DAB2umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.0165692242010NA540410482TC
rs1180530317554300149233IL23Rumls:C0010346GWASCATGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.0.3705974352007IL23R167209833CT
rs1187180121102463284119PTRFumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1223670322010PTRF1742418754AC
rs11924265255579509223MAGI1umls:C0010346GWASCATIdentification of risk loci for Crohn's disease phenotypes using a genome-wide association study.0.122014MAGI1365774667TC
rs11938228247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014TLR24153700794CA
rs11938228247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014TLR24153700794CA
rs119382282477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR24153700794CA
rs11938228247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014TLR24153700794CA
rs11938228247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014TLR24153700794CA
rs11938228247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014TLR24153700794CA
rs11938228247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014TLR24153700794CA
rs11938228247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR24153700794CA
rs11938228247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014TLR24153700794CA
rs11938228247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014TLR24153700794CA
rs11938228247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014TLR24153700794CA
rs119382282477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014TLR24153700794CA
rs12003322525951111177BAZ1Aumls:C0010346BeFreeWe also observed suggestive evidence for the association of the BAZ1A promoter SNP with CD (rs1200332, 0.45 in CD, 0.35 in controls, OR 1.5, p = 2×10-6).0.0002714422014NA1434897929TC
rs1203508217554261356FASLGumls:C0010346GAD[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]0.0123780442007NA1172929237TC
rs12212067240351922309FOXO3umls:C0010346BeFreeWe identify a noncoding polymorphism in FOXO3A (rs12212067: T > G) at which the minor (G) allele, despite not being associated with disease susceptibility, is associated with a milder course of Crohn's disease and rheumatoid arthritis and with increased risk of severe malaria.0.0008143262013FOXO36108659993TG
rs122120672536524964127NOD2umls:C0010346BeFreeThe NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.0.562014FOXO36108659993TG
rs12212067253652492309FOXO3umls:C0010346BeFreeThe NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.0.0008143262014FOXO36108659993TG
rs1224211021102463219771CCNYumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.2569265422010CCNY1035246767AG
rs12377632249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014TLR49117710452TC
rs12377632249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014TLR49117710452TC
rs12377632249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014TLR49117710452TC
rs12505442248280457178ZMIZ1umls:C0010346GWASCATWe identified seven susceptibility loci outside the human leukocyte antigen region (9p24 near JAK2, 10q22 at ZMIZ1, 11q13 near PRDX5, 16p13 near SOCS1, 17q21 at STAT3, 19p13 near FUT2, and 22q11 at YDJC) shared between PS and CD with genome-wide significance (p < 5 × 10(-8)) and confirmed four already established PS and CD risk loci (IL23R, IL12B, REL, and TYK2).0.1250055062012ZMIZ11079273128GA
rs12505502110246357178ZMIZ1umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1250055062010ZMIZ11079300560CA
rs12505502110246357178ZMIZ1umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1250055062010ZMIZ11079300560CA
rs12505692548996057178ZMIZ1umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1250055062015ZMIZ11079285450TC
rs1250569254899602859GPR35umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0002714422015ZMIZ11079285450TC
rs12505692548996029761USP25umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0026384742015ZMIZ11079285450TC
rs125056925489960159296NKX2-3umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2743860362015ZMIZ11079285450TC
rs12505692548996022891ZNF365umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1373835492015ZMIZ11079285450TC
rs1250569254899605771PTPN2umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2690232122015ZMIZ11079285450TC
rs1252186821102463441108C5orf56umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1271010962010C5orf565132448701GT
rs1252186821102463441108C5orf56umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1271010962010C5orf565132448701GT
rs1267766322412388157869SBSPONumls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.1223670322012SBSPON873095112GT
rs1267766322412388157869SBSPONumls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.1223670322012SBSPON873095112GT
rs12720356211024637297TYK2umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.2450055062010TYK21910359299AC
rs12720356211024637297TYK2umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.2450055062010TYK21910359299AC
rs12721602218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NR1I23119781009GA
rs12721607218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NR1I23119807356GA
rs12722489211024633559IL2RAumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.245548392010IL2RA106060049CT
rs12722489211024633559IL2RAumls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.245548392010IL2RA106060049CT
rs1297265235110343717JAK2umls:C0010346BeFreeFOS, UBE2L3, the JAK2 gene region, and rs1297265 at chromosome arm 21q21.1 likely play a role in both Crohn's disease and UC.0.0140066952013LOC1019277452115444732AG
rs129949972312823355054ATG16L1umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.3678631532012ATG16L12233264857GA
rs1300346422412388150962PUS10umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.1273725382012PUS10260959694AG
rs1300346422412388150962PUS10umls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.1273725382012PUS10260959694AG
rs13073817211024636304SATB1umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.0023670322010NA318665366GA
rs131265052312823355024BANK1umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012BANK14101944147GA
rs1336118919491842345611IRGMumls:C0010346BeFreeThe aim of this study was to determine the role of the ATG16L1 (rs2241880) and IRGM (rs13361189 and rs4958847) genes polymorphism in Crohn's disease (CD) and ulcerative colitis (UC).0.170269082009NA5150843825TC
rs133611891949184255054ATG16L1umls:C0010346BeFreeThe aim of this study was to determine the role of the ATG16L1 (rs2241880) and IRGM (rs13361189 and rs4958847) genes polymorphism in Crohn's disease (CD) and ulcerative colitis (UC).0.3678631532009NA5150843825TC
rs133611891755426185027SMIM3umls:C0010346GAD[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]0.0023670322007NA5150843825TC
rs13428812211024631788DNMT3Aumls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.2423670322010DNMT3A225269598AG
rs13428812211024631788DNMT3Aumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.2423670322010DNMT3A225269598AG
rs134315117804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167253446GA
rs1373692174478421601DAB2umls:C0010346GAD[Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.]0.0165692242007NA540431081AC
rs139802418723019256815C10orf67umls:C0010346GAD[Our study demonstrates that the combined analysis of different, albeit clinically related, phenotypes can lead to the identification of common susceptibility loci.]0.0023670322008NA1023376509GT
rs1405655212459924790NFKB1umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0082628082011NR1H21950379362TC
rs1405655212459928856NR1I2umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0069914752011NR1H21950379362TC
rs145689318587394100130988C7orf72umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0023670322008NA750230076GA
rs145922845128258693586IL10umls:C0010346BeFreeA Gly15Arg mutation in the interleukin-10 gene reduces secretion of interleukin-10 in Crohn disease.0.1655250852003IL101206772393CT
rs151181211024631201CLN3umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1223670322010CLN3;NPIPB81628479196TC
rs151181211024631201CLN3umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1223670322010CLN3;NPIPB81628479196TC
rs1523127212459924790NFKB1umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0082628082011NR1I23119782192CA
rs1523127218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NR1I23119782192CA
rs1523127212459928856NR1I2umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0069914752011NR1I23119782192CA
rs1523128218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NR1I23119781817AG
rs15513981858739410221TRIB1umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0071010962008LOC1053757458125527809GA
rs1554973247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014NA9117718534TC
rs1554973249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014NA9117718534TC
rs1554973247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014NA9117718534TC
rs1554973247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014NA9117718534TC
rs1554973247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014NA9117718534TC
rs1554973247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014NA9117718534TC
rs15549732477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014NA9117718534TC
rs1554973247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014NA9117718534TC
rs1554973249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014NA9117718534TC
rs1554973247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014NA9117718534TC
rs1554973249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014NA9117718534TC
rs1554973247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014NA9117718534TC
rs1554973247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014NA9117718534TC
rs15549732477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014NA9117718534TC
rs1554973247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014NA9117718534TC
rs1568885247071447124TNFumls:C0010346BeFreeAssociation of rs1568885, rs1813443 and rs4411591 polymorphisms with anti-TNF medication response in Greek patients with Crohn's disease.0.4222949572014NA713597906TA
rs172214171755430064127NOD2umls:C0010346GWASCATGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.0.562007NOD21650705671CG
rs17234657175543001601DAB2umls:C0010346GAD[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]0.0165692242007NA540401407TG
rs17293632211024634088SMAD3umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.2426384742010SMAD31567150258CT
rs17293632211024634088SMAD3umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.2426384742010SMAD31567150258CT
rs173098272110246363027SLC22A23umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.131835162010SLC22A2363433084TG
rs173098272110246363027SLC22A23umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.131835162010SLC22A2363433084TG
rs1731326525259511149233IL23Rumls:C0010346BeFreeWe observed the association between Crohn's disease and NOD2 (rs17313265, 0.28 in CD, 0.19 in controls, OR 1.5, p = 9×10-6) and IL23R (rs11209026, 0.026 in CD, 0.0.071 in controls, OR 0.4, p = 3.8×10-4).0.3705974352014NOD21650713793CT
rs173132652525951164127NOD2umls:C0010346BeFreeWe observed the association between Crohn's disease and NOD2 (rs17313265, 0.28 in CD, 0.19 in controls, OR 1.5, p = 9×10-6) and IL23R (rs11209026, 0.026 in CD, 0.0.071 in controls, OR 0.4, p = 3.8×10-4).0.562014NOD21650713793CT
rs1736135185873948204NRIP1umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0023670322008LOC1019277452115432901TC
rs176950922312823380315CPEB4umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.1223670322012CPEB45173910850TG
rs1793004176845444745NELL1umls:C0010346GAD[Subsequent fine mapping and replication in an independent sample of 454 French/Canadian CD trios supported the authenticity of the NELL1 association.]0.0050055062007NELL11120677383CG
rs1799964211024637124TNFumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.4222949572010LTA;TNF;LOC100287329631574531TC
rs1799964211024634049LTAumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1309112142010LTA;TNF;LOC100287329631574531TC
rs1800629249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014TNF631575254GA
rs1800629249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014TNF631575254GA
rs1800629249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014TNF631575254GA
rs1801282249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014PPARG312351626CG
rs1801282249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014PPARG312351626CG
rs1801282249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014PPARG312351626CG
rs1813443247071447124TNFumls:C0010346BeFreeAssociation of rs1568885, rs1813443 and rs4411591 polymorphisms with anti-TNF medication response in Greek patients with Crohn's disease.0.4222949572014CNTN511100140279GC
rs181359211024637332UBE2L3umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1250055062010UBE2L32221574352GA
rs181359211024637332UBE2L3umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1250055062010UBE2L32221574352GA
rs1816702247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014TLR24153688371TC
rs18167022477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR24153688371TC
rs1816702247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014TLR24153688371TC
rs1816702247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014TLR24153688371TC
rs1816702247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014TLR24153688371TC
rs1816702247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014TLR24153688371TC
rs1816702249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014TLR24153688371TC
rs18167022477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014TLR24153688371TC
rs1816702249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014TLR24153688371TC
rs1816702247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014TLR24153688371TC
rs1816702247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014TLR24153688371TC
rs1816702247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014TLR24153688371TC
rs1816702247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014TLR24153688371TC
rs1816702249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014TLR24153688371TC
rs1816702247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR24153688371TC
rs1818566152019548056144PCDHA4umls:C0010346BeFreeThe cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's disease.0.0002714422010PCDHA9;PCDHA11;PCDHA10;PCDHA8;PCDHA7;PCDHA6;PCDHA5;PCDHA4;PCDHA3;PCDHA2;PCDHA15140870462GA
rs18474722110246360468BACH2umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.2429099162010BACH2690263440CA
rs18474722110246360468BACH2umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.2429099162010BACH2690263440CA
rs1861494251715103458IFNGumls:C0010346BeFreePeripheral T cells of UC and Crohn's disease (CD) patients were genotyped for rs1861494 and analyzed for allele-specific and IFNG promoter methylation.0.1303346542015IFNG1268157629CT
rs187084247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014TLR9352227015AG
rs187084247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014TLR9352227015AG
rs187084247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014TLR9352227015AG
rs187084247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014TLR9352227015AG
rs187084247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014TLR9352227015AG
rs187084247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014TLR9352227015AG
rs187084247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR9352227015AG
rs187084247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014TLR9352227015AG
rs187084247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014TLR9352227015AG
rs1870842477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014TLR9352227015AG
rs1870842477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR9352227015AG
rs187084247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014TLR9352227015AG
rs1893217211024635771PTPN2umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.2690232122010PTPN21812809341AG
rs19064932241238810221TRIB1umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.0071010962012NA8126080638GT
rs1919013941861777964127NOD2umls:C0010346BeFreeOur aim was to evaluate the frequency of CX3CR1 V249I and T280M polymorphisms and NOD2/CARD15 mutations in Crohn's disease patients and to search for a relationship with phenotype.0.562008NOD21650710831CT
rs1992660176845441601DAB2umls:C0010346GAD[Systematic association mapping identifies NELL1 as a novel IBD disease gene.]0.0165692242007NA540414965CT
rs1992660176845445734PTGER4umls:C0010346GAD[Systematic association mapping identifies NELL1 as a novel IBD disease gene.]0.0185551932007NA540414965CT
rs199859821102463163486DENND1Bumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.2423670322010DENND1B1197758512AG
rs199859821102463163486DENND1Bumls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.2423670322010DENND1B1197758512AG
rs20240922312823322904SBNO2umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.1247340642012SBNO2191124032GA
rs2032582156855405243ABCB1umls:C0010346BeFreeThis was a case-control analysis of MDR1 C3435T and G2677T SNPs in a large well-characterized Scottish white cohort (335 with ulcerative colitis [UC], 268 with Crohn's disease [CD], and 370 healthy controls).0.0260036762005ABCB1787531302AT,C
rs2032582172603535243ABCB1umls:C0010346BeFreeA total of 211 patients with Crohn's disease (CD), 97 patients with ulcerative colitis (UC), and 212 control subjects were investigated for the presence of MDR1 G2677T/A and C3435T polymorphisms.0.0260036762007ABCB1787531302AT,C
rs2032582166330485243ABCB1umls:C0010346BeFreeThe present study examined the association of ABCB1 C3435T and G2677T/A in a large British case-control cohort of 828 Crohn's disease, 580 ulcerative colitis (UC) cases, and 285 healthy controls.0.0260036762006ABCB1787531302AT,C
rs2032582191151525243ABCB1umls:C0010346BeFreeIn this study, the G2677T/A polymorphism observed in the MDR1 gene was not found to be a risk factor for Crohn's disease or ulcerative colitis.0.0260036762008ABCB1787531302AT,C
rs204321120182451114548NLRP3umls:C0010346BeFreeEvidence of interaction of CARD8 rs2043211 with NALP3 rs35829419 in Crohn's disease.0.1408126052010CARD81948234449AT
rs20432111809234422900CARD8umls:C0010346BeFreeNo association of the CARD8 (TUCAN) c.30T>A (p.C10X) variant with Crohn's disease: a study in 3 independent European cohorts.0.0085441822008CARD81948234449AT
rs20432112018245164127NOD2umls:C0010346BeFreeWe found that the presence of the minor allele of rs2043211 with the major allele of rs35829419 conferred a protective effect against Crohn's disease (and vice versa), which intensified in the absence of NOD2 mutations (P(1,2/1,1)=0.009, odds ratio (OR)=0.66, 95% confidence interval (CI) (0.48-0.90); P(1,1/1,2)=0.015, OR=0.35, 95% CI (0.15-0.82)).0.562010CARD81948234449AT
rs20432112018245122900CARD8umls:C0010346BeFreeEvidence of interaction of CARD8 rs2043211 with NALP3 rs35829419 in Crohn's disease.0.0085441822010CARD81948234449AT
rs20432112018245122900CARD8umls:C0010346GAD[Evidence of interaction of CARD8 rs2043211 with NALP3 rs35829419 in Crohn's disease.]0.0085441822010CARD81948234449AT
rs20432112350654322900CARD8umls:C0010346BeFreeThe CARD8 p.C10X mutation associates with a low anti-glycans antibody response in patients with Crohn's disease.0.0085441822013CARD81948234449AT
rs2058660211024638807IL18RAPumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.129739572010IL18RAP2102437989GA
rs2058660211024638807IL18RAPumls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.129739572010IL18RAP2102437989GA
rs206468917804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167187327GA
rs2066842187155156583SLC22A4umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.0796595422008NOD21650710713CA,T
rs20668421871551564127NOD2umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.562008NOD21650710713CA,T
rs2066842187155156584SLC22A5umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.0796694742008NOD21650710713CA,T
rs20668421871551555054ATG16L1umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.3678631532008NOD21650710713CA,T
rs20668421211519564127NOD2umls:C0010346BeFreeA case-control study of NOD2 polymorphisms known to be associated with Crohn's disease (CD) (Pro(268)Ser, Arg(702)Trp, Gly(908)Arg, and Leu(1007)fsinsC) was performed in 229 cases of primary AS with no diagnosed inflammatory bowel disease (IBD), 197 cases of AS associated with IBD (referred to as colitic spondylarthritis; comprising 78 with CD and 119 with ulcerative colitis [UC]), and 229 ethnically matched, healthy controls.0.562002NOD21650710713CA,T
rs20668432120993864127NOD2umls:C0010346BeFreeThe NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.0.562010NOD21650711288CA,T
rs20668441854193064127NOD2umls:C0010346BeFreeThe R702W mutation of CARD15 gene was associated with Crohn's disease in the Iranian population.0.562008NOD21650712015CT
rs20668441681997064127NOD2umls:C0010346BeFreeIn cells carrying the Crohn-associated NOD2 variant R702W the NF-kappaB response was significantly diminished.0.562006NOD21650712015CT
rs20668442008248364127NOD2umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.562010NOD21650712015CT
rs20668441552732464127NOD2umls:C0010346BeFreeThree mutations (R702W, G908R, and 1007fs) within the CARD15 gene have been identified as independent risk factors for the development of Crohn's disease (CD).0.562004NOD21650712015CT
rs20668441520278464127NOD2umls:C0010346BeFreeA frameshift mutation (Leu1007fsinsC) and two missense mutations (Gly908Arg and Arg702Trp) in the NOD2/CARD15 gene are strongly associated with susceptibility to Crohn's disease.0.562004NOD21650712015CT
rs20668441735596864127NOD2umls:C0010346BeFreeIn this study, we demonstrate that membrane-bound versions of NOD2 and Crohn disease-associated mutants R702W and G908R are capable of responding to MDP and activating the NF-kappaB pathway from this location.0.562007NOD21650712015CT
rs20668441211519564127NOD2umls:C0010346BeFreeA case-control study of NOD2 polymorphisms known to be associated with Crohn's disease (CD) (Pro(268)Ser, Arg(702)Trp, Gly(908)Arg, and Leu(1007)fsinsC) was performed in 229 cases of primary AS with no diagnosed inflammatory bowel disease (IBD), 197 cases of AS associated with IBD (referred to as colitic spondylarthritis; comprising 78 with CD and 119 with ulcerative colitis [UC]), and 229 ethnically matched, healthy controls.0.562002NOD21650712015CT
rs20668442169008864127NOD2umls:C0010346BeFreeWe also show that the three main Crohn disease-associated mutants of NOD2 (1007fs, R702W, G908R) form an interaction with RIG-I and negatively regulate its signaling to a greater extent than wild-type NOD2.0.562011NOD21650712015CT
rs20668441735596819ABCA1umls:C0010346BeFreeIn this study, we demonstrate that membrane-bound versions of NOD2 and Crohn disease-associated mutants R702W and G908R are capable of responding to MDP and activating the NF-kappaB pathway from this location.0.0005428842007NOD21650712015CT
rs20668441957005264127NOD2umls:C0010346BeFreeNOD2/CARD15 is involved in the innate immune response and three polymorphisms in this gene (Arg702Trp rs2066844, Gly908Arg rs2066845 and Leu1007fsinsC rs5743293) have been associated with risk of the rare Crohn's disease.0.562010NOD21650712015CT
rs206684420082483149233IL23Rumls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3705974352010NOD21650712015CT
rs20668441613396964127NOD2umls:C0010346BeFreeFurthermore, the three main mutations of CARD15/NOD2 (R702W, G908R, and 1007fs) associated with susceptibility to Crohn's disease were not found in these patients.0.562005NOD21650712015CT
rs206684412019468317APAF1umls:C0010346BeFreeCARD15 is related to the NOD1/Apaf-1 family of apoptosis regulators, and three sequence variants (Arg702Trp, Gly908Arg, and Leu1007fsinsC) in the gene were demonstrated to be associated with CD.0.0002714422002NOD21650712015CT
rs20668442008248355054ATG16L1umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3678631532010NOD21650712015CT
rs20668441861657664127NOD2umls:C0010346BeFreeGranulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702W.0.562008NOD21650712015CT
rs2066844187155156584SLC22A5umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.0796694742008NOD21650712015CT
rs20668441476277764127NOD2umls:C0010346BeFreeSera from 303 patients were tested for antibodies to the Crohn's disease-related bacterial sequence (I2), anti-Escherichia coli outer membrane porin C, anti-Saccharomyces cerevisiae, and perinuclear antineutrophil cytoplasmic antibodies and for 3 Crohn's disease-associated variants of the NOD2 gene (R702W, G908R, and 1007fs) and compared with clinical data.0.562004NOD21650712015CT
rs20668441871551564127NOD2umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.562008NOD21650712015CT
rs20668441871551555054ATG16L1umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.3678631532008NOD21650712015CT
rs2066844187155156583SLC22A4umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.0796595422008NOD21650712015CT
rs20668441578531864127NOD2umls:C0010346BeFreeThree common NOD2 mutations -- 3020insC, G908R and R702W -- have been shown to be associated with chronic inflammatory disease such as Crohn's disease, the 3020insC also with human malignancy colorectal cancer.0.562005NOD21650712015CT
rs20668442434542364127NOD2umls:C0010346BeFreeThree NOD2 polymorphisms (single nucleotide polymorphism [SNP]8 [2104C>T, Arg702Trp], SNP12 [2722G>C, Gly908Arg], and SNP13 [3020insC, Leu1007 fsins C]), identified as disease-associated variants in Crohn's disease, have recently been suggested as gene markers of the outcome of hematopoietic stem cell transplantation (HSCT).0.562013NOD21650712015CT
rs20668441868022364127NOD2umls:C0010346BeFreeTo evaluate the role of genetic factors in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC), we investigated the single nucleotide polymorphisms (SNPs) of NOD2/CARD15 (R702W, G908R and L1007finsC), and Toll-like receptor 4 (TLR4) genes (D299G and T399I) in a selected inflammatory bowel disease (IBD) population coming from Southern Italy.0.562008NOD21650712015CT
rs20668441516881164127NOD2umls:C0010346BeFreeCARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease.0.562004NOD21650712015CT
rs20668442389259064127NOD2umls:C0010346BeFreeActivation of NOD2 in HEK293 cells overexpressing NOD2 induced the IL-17C promoter, an activity that was significantly reduced in cells overexpressing the Crohn's disease-associated NOD2 mutation 3020insC (1007fs) or the Crohn's disease- and atopic dermatitis-associated NOD2-R702W variant.0.562013NOD21650712015CT
rs20668441974896464127NOD2umls:C0010346BeFreeIt has been shown previously that three nucleotide-binding oligomerization domain containing 2 (NOD2) variants (Arg702Trp, Gly908Arg and Lue1007fs) are associated with Crohn's disease (CD), a disorder clinically resembling Behçet's disease (BD).0.562009NOD21650712015CT
rs20668442389259027189IL17Cumls:C0010346BeFreeActivation of NOD2 in HEK293 cells overexpressing NOD2 induced the IL-17C promoter, an activity that was significantly reduced in cells overexpressing the Crohn's disease-associated NOD2 mutation 3020insC (1007fs) or the Crohn's disease- and atopic dermatitis-associated NOD2-R702W variant.0.0008143262013NOD21650712015CT
rs2066844186802237099TLR4umls:C0010346BeFreeTo evaluate the role of genetic factors in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC), we investigated the single nucleotide polymorphisms (SNPs) of NOD2/CARD15 (R702W, G908R and L1007finsC), and Toll-like receptor 4 (TLR4) genes (D299G and T399I) in a selected inflammatory bowel disease (IBD) population coming from Southern Italy.0.1828426212008NOD21650712015CT
rs20668441648512464127NOD2umls:C0010346BeFreeWe performed a limited DNA sequence analysis of the CARD15 gene in 89 patients with Crohn's disease (CD), 19 patients with ulcerative colitis (UC), and three patients with indeterminate colitis (IC), who were heterozygous carriers of one of the common CARD15 mutations [c.2104C>T (p.R702W), c.2722G>C (p.G908R), or c.3019_3020insC (p.Leu1007fsX1008)], the c.2462+10A>C variant, or of a new amino acid substitution in the 3'-end of exon 4.0.562006NOD21650712015CT
rs20668441536719464127NOD2umls:C0010346BeFreeTwo functional mutations, an insertion mutation at nucleotide 3020 (3020insC) and a missense mutation C2104T in the CARD15 gene (originally NOD2 gene) have been reported to be associated with Crohn's disease.0.562004NOD21650712015CT
rs20668442254315764127NOD2umls:C0010346BeFreeOnly two patients with early onset Crohn's disease exhibited rare deleterious variations within NOD2: the previously described R702W variant was the sole NOD2 variant in one patient, while the second patient also carried the L1007 frameshift insertion.0.562013NOD21650712015CT
rs20668442228921164127NOD2umls:C0010346BeFreeCrohn's disease-associated NOD 2 variants (Arg702Trp and 3020insC) were found to be monomorphic (wild), and 7 subjects were heterozygous for Gly908Arg SNP in 263 patients with tuberculosis, 260 patients with leprosy and 270 healthy controls residing in northern Indian states.0.562012NOD21650712015CT
rs20668441201946810392NOD1umls:C0010346BeFreeCARD15 is related to the NOD1/Apaf-1 family of apoptosis regulators, and three sequence variants (Arg702Trp, Gly908Arg, and Leu1007fsinsC) in the gene were demonstrated to be associated with CD.0.0170883632002NOD21650712015CT
rs20668441766191364127NOD2umls:C0010346BeFreeGenomic DNA from 563 individuals (Crohn's disease: n = 205; ulcerative colitis: n = 154; controls: n = 204) was analyzed for the presence of the SELS-105G>A polymorphism and the three nucleotide-binding oligomerization domain-containing protein 2 (NOD2)/caspase recruitment domain-containing protein 15 (CARD15) variants p.Arg702Trp, p.Gly908Arg and p.Leu1007fsX1008.0.562007NOD21650712015CT
rs20668441717442664127NOD2umls:C0010346BeFreeIn the current study, the frequency of CARD15/NOD2 gene variants (R702W, G908R, L1007fs), previously associated with Crohn's disease--a common inflammatory bowel disease, have been examined in a group of 308 sporadic PD patients and 220 healthy controls.0.562007NOD21650712015CT
rs20668442064600264127NOD2umls:C0010346BeFreeParticular mutations of the NOD2 gene are associated with Crohn's disease including gly908arg, leu1007finsc and arg702trp polymorphisms.0.562010NOD21650712015CT
rs20668451748905464127NOD2umls:C0010346BeFreeIn the Dutch population, CARD15 G908R and L1007fs are associated with Crohn's disease.0.562007NOD21650722629GC,T
rs206684512019468317APAF1umls:C0010346BeFreeCARD15 is related to the NOD1/Apaf-1 family of apoptosis regulators, and three sequence variants (Arg702Trp, Gly908Arg, and Leu1007fsinsC) in the gene were demonstrated to be associated with CD.0.0002714422002NOD21650722629GC,T
rs20668451516881164127NOD2umls:C0010346BeFreeCARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease.0.562004NOD21650722629GC,T
rs20668452008248364127NOD2umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.562010NOD21650722629GC,T
rs20668451894275464127NOD2umls:C0010346BeFreeOur aim was to investigate associations among IL1B-511, IL1B-31, IL1RN, TNFA-307, TLR-2, TLR-4, IL2-330, NOD2 G908R, NOD2 L1007fsinsC polymorphisms and both Crohn's disease (CD) and ulcerative colitis (UC) in a Brazilian population.0.562009NOD21650722629GC,T
rs20668452169008864127NOD2umls:C0010346BeFreeWe also show that the three main Crohn disease-associated mutants of NOD2 (1007fs, R702W, G908R) form an interaction with RIG-I and negatively regulate its signaling to a greater extent than wild-type NOD2.0.562011NOD21650722629GC,T
rs20668451735596864127NOD2umls:C0010346BeFreeIn this study, we demonstrate that membrane-bound versions of NOD2 and Crohn disease-associated mutants R702W and G908R are capable of responding to MDP and activating the NF-kappaB pathway from this location.0.562007NOD21650722629GC,T
rs20668451201946810392NOD1umls:C0010346BeFreeCARD15 is related to the NOD1/Apaf-1 family of apoptosis regulators, and three sequence variants (Arg702Trp, Gly908Arg, and Leu1007fsinsC) in the gene were demonstrated to be associated with CD.0.0170883632002NOD21650722629GC,T
rs20668451613396964127NOD2umls:C0010346BeFreeFurthermore, the three main mutations of CARD15/NOD2 (R702W, G908R, and 1007fs) associated with susceptibility to Crohn's disease were not found in these patients.0.562005NOD21650722629GC,T
rs20668451727812664127NOD2umls:C0010346BeFreeRole of ASCA and the NOD2/CARD15 mutation Gly908Arg in predicting increased surgical costs in Crohn's disease patients: a project of the European Collaborative Study Group on Inflammatory Bowel Disease.0.562007NOD21650722629GC,T
rs20668451552732464127NOD2umls:C0010346BeFreeThree mutations (R702W, G908R, and 1007fs) within the CARD15 gene have been identified as independent risk factors for the development of Crohn's disease (CD).0.562004NOD21650722629GC,T
rs20668451578531864127NOD2umls:C0010346BeFreeThree common NOD2 mutations -- 3020insC, G908R and R702W -- have been shown to be associated with chronic inflammatory disease such as Crohn's disease, the 3020insC also with human malignancy colorectal cancer.0.562005NOD21650722629GC,T
rs20668451735596819ABCA1umls:C0010346BeFreeIn this study, we demonstrate that membrane-bound versions of NOD2 and Crohn disease-associated mutants R702W and G908R are capable of responding to MDP and activating the NF-kappaB pathway from this location.0.0005428842007NOD21650722629GC,T
rs20668451520278464127NOD2umls:C0010346BeFreeA frameshift mutation (Leu1007fsinsC) and two missense mutations (Gly908Arg and Arg702Trp) in the NOD2/CARD15 gene are strongly associated with susceptibility to Crohn's disease.0.562004NOD21650722629GC,T
rs20668451259590664127NOD2umls:C0010346BeFreeAn insertion mutation at nucleotide 3020 (3020insC) and a missense mutation G2722C in the CARD15 gene on chromosome 16p have been reported to be associated with Crohn's disease (CD).0.562003NOD21650722629GC,T
rs20668451648512464127NOD2umls:C0010346BeFreeWe performed a limited DNA sequence analysis of the CARD15 gene in 89 patients with Crohn's disease (CD), 19 patients with ulcerative colitis (UC), and three patients with indeterminate colitis (IC), who were heterozygous carriers of one of the common CARD15 mutations [c.2104C>T (p.R702W), c.2722G>C (p.G908R), or c.3019_3020insC (p.Leu1007fsX1008)], the c.2462+10A>C variant, or of a new amino acid substitution in the 3'-end of exon 4.0.562006NOD21650722629GC,T
rs206684520082483149233IL23Rumls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3705974352010NOD21650722629GC,T
rs2066845186802237099TLR4umls:C0010346BeFreeTo evaluate the role of genetic factors in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC), we investigated the single nucleotide polymorphisms (SNPs) of NOD2/CARD15 (R702W, G908R and L1007finsC), and Toll-like receptor 4 (TLR4) genes (D299G and T399I) in a selected inflammatory bowel disease (IBD) population coming from Southern Italy.0.1828426212008NOD21650722629GC,T
rs20668452228921164127NOD2umls:C0010346BeFreeCrohn's disease-associated NOD 2 variants (Arg702Trp and 3020insC) were found to be monomorphic (wild), and 7 subjects were heterozygous for Gly908Arg SNP in 263 patients with tuberculosis, 260 patients with leprosy and 270 healthy controls residing in northern Indian states.0.562012NOD21650722629GC,T
rs20668451717442664127NOD2umls:C0010346BeFreeIn the current study, the frequency of CARD15/NOD2 gene variants (R702W, G908R, L1007fs), previously associated with Crohn's disease--a common inflammatory bowel disease, have been examined in a group of 308 sporadic PD patients and 220 healthy controls.0.562007NOD21650722629GC,T
rs20668452434542364127NOD2umls:C0010346BeFreeThree NOD2 polymorphisms (single nucleotide polymorphism [SNP]8 [2104C>T, Arg702Trp], SNP12 [2722G>C, Gly908Arg], and SNP13 [3020insC, Leu1007 fsins C]), identified as disease-associated variants in Crohn's disease, have recently been suggested as gene markers of the outcome of hematopoietic stem cell transplantation (HSCT).0.562013NOD21650722629GC,T
rs20668452064600264127NOD2umls:C0010346BeFreeParticular mutations of the NOD2 gene are associated with Crohn's disease including gly908arg, leu1007finsc and arg702trp polymorphisms.0.562010NOD21650722629GC,T
rs20668451766191364127NOD2umls:C0010346BeFreeGenomic DNA from 563 individuals (Crohn's disease: n = 205; ulcerative colitis: n = 154; controls: n = 204) was analyzed for the presence of the SELS-105G>A polymorphism and the three nucleotide-binding oligomerization domain-containing protein 2 (NOD2)/caspase recruitment domain-containing protein 15 (CARD15) variants p.Arg702Trp, p.Gly908Arg and p.Leu1007fsX1008.0.562007NOD21650722629GC,T
rs20668452370915764127NOD2umls:C0010346BeFreeThree common NOD2 mutations are associated with Crohn's disease (p=5.08×10(-7), 1.67×10(-6), and 1.87×10(-2) for 1007fs, R720W, and G908R, respectively), but not with ulcerative colitis (p=0.1046, 0.1269, and 0.8929, respectively).0.562013NOD21650722629GC,T
rs20668451211519564127NOD2umls:C0010346BeFreeA case-control study of NOD2 polymorphisms known to be associated with Crohn's disease (CD) (Pro(268)Ser, Arg(702)Trp, Gly(908)Arg, and Leu(1007)fsinsC) was performed in 229 cases of primary AS with no diagnosed inflammatory bowel disease (IBD), 197 cases of AS associated with IBD (referred to as colitic spondylarthritis; comprising 78 with CD and 119 with ulcerative colitis [UC]), and 229 ethnically matched, healthy controls.0.562002NOD21650722629GC,T
rs20668451868022364127NOD2umls:C0010346BeFreeTo evaluate the role of genetic factors in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC), we investigated the single nucleotide polymorphisms (SNPs) of NOD2/CARD15 (R702W, G908R and L1007finsC), and Toll-like receptor 4 (TLR4) genes (D299G and T399I) in a selected inflammatory bowel disease (IBD) population coming from Southern Italy.0.562008NOD21650722629GC,T
rs20668451957005264127NOD2umls:C0010346BeFreeNOD2/CARD15 is involved in the innate immune response and three polymorphisms in this gene (Arg702Trp rs2066844, Gly908Arg rs2066845 and Leu1007fsinsC rs5743293) have been associated with risk of the rare Crohn's disease.0.562010NOD21650722629GC,T
rs20668451476277764127NOD2umls:C0010346BeFreeSera from 303 patients were tested for antibodies to the Crohn's disease-related bacterial sequence (I2), anti-Escherichia coli outer membrane porin C, anti-Saccharomyces cerevisiae, and perinuclear antineutrophil cytoplasmic antibodies and for 3 Crohn's disease-associated variants of the NOD2 gene (R702W, G908R, and 1007fs) and compared with clinical data.0.562004NOD21650722629GC,T
rs20668451974896464127NOD2umls:C0010346BeFreeIt has been shown previously that three nucleotide-binding oligomerization domain containing 2 (NOD2) variants (Arg702Trp, Gly908Arg and Lue1007fs) are associated with Crohn's disease (CD), a disorder clinically resembling Behçet's disease (BD).0.562009NOD21650722629GC,T
rs20668452008248355054ATG16L1umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3678631532010NOD21650722629GC,T
rs20668472536524964127NOD2umls:C0010346BeFreeThe NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.0.562014NOD21650729867-C
rs20668472312823364127NOD2umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.562012NOD21650729867-C
rs206684720082483149233IL23Rumls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3705974352010NOD21650729867-C
rs20668471858739464127NOD2umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.562008NOD21650729867-C
rs20668472057096664127NOD2umls:C0010346GWASCATFucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.0.562010NOD21650729867-C
rs20668472008248364127NOD2umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.562010NOD21650729867-C
rs2066847253652492309FOXO3umls:C0010346BeFreeThe NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.0.0008143262014NOD21650729867-C
rs20668472008248355054ATG16L1umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3678631532010NOD21650729867-C
rs20758201796487010392NOD1umls:C0010346BeFreeNOD1 gene E266K polymorphism is associated with disease susceptibility but not with disease phenotype or NOD2/CARD15 in Hungarian patients with Crohn's disease.0.0170883632007NOD1730452621CT
rs20758201796487064127NOD2umls:C0010346BeFreeNOD1 gene E266K polymorphism is associated with disease susceptibility but not with disease phenotype or NOD2/CARD15 in Hungarian patients with Crohn's disease.0.562007NOD1730452621CT
rs20767562293666964127NOD2umls:C0010346GWASCATA genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.0.562013NOD21650722970AG
rs20767562120993864127NOD2umls:C0010346BeFreeThe NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.0.562010NOD21650722970AG
rs20767562110246364127NOD2umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.562010NOD21650722970AG
rs20767562241238864127NOD2umls:C0010346GWASCATIn all, the 16 replicated and newly discovered loci, in addition to the three coding NOD2 variants, accounted for 11.2% of the total genetic variance for CD risk in the AJ population.0.562012NOD21650722970AG
rs20767561743575664127NOD2umls:C0010346GWASCATGenome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.0.562007NOD21650722970AG
rs20767561768454464127NOD2umls:C0010346GWASCATAmong the 116,161 single-nucleotide polymorphisms tested, an association with the known CD susceptibility gene NOD2, the 5q31 haplotype, and the recently reported CD locus at 5p13.1 was confirmed.0.562007NOD21650722970AG
rs208294172572215027P2RX7umls:C0010346BeFreeFunctional P2X7 receptor polymorphisms (His155Tyr, Arg307Gln, Glu496Ala) in patients with Crohn's disease.0.0008143262007P2RX7;LOC10537003212121162450TG,C,A
rs21238821102463117289TAGAPumls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1231813582010NA6159069404CT
rs2149085238507138635RNASET2umls:C0010346GWASCATGenome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.0.1223670322014RNASET26166957622TC
rs2165047174766809231DLG5umls:C0010346GAD[Polymorphisms 3020insC in CARD15 and SNP rs3792876 in SLC22A4/5 occurred statistically significantly more often in patients with pediatric-onset CD than in patients with adult-onset CD. Polymorphisms 3020insC in CARD15 and SNP rs2165047 in DLG5 were assoc]0.0570089772007DLG51077791882CT
rs218896218587394441108C5orf56umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.1271010962008C5orf565132435113CT
rs218896220570966441108C5orf56umls:C0010346GWASCATFucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.0.1271010962010C5orf565132435113CT
rs218896218587394441108C5orf56umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1271010962008C5orf565132435113CT
rs218896220570966441108C5orf56umls:C0010346GAD[Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.]0.1271010962010C5orf565132435113CT
rs22018412006673664127NOD2umls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.562010IL23R167228519AG
rs22018412006673655054ATG16L1umls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.3678631532010IL23R167228519AG
rs22018412006673650941IBD5umls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.0496165762010IL23R167228519AG
rs220184120066736149233IL23Rumls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.3705974352010IL23R167228519AG
rs220184117804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167228519AG
rs2229113127594363587IL10RAumls:C0010346BeFreeWe decided to screen for mutations of the IL-10R1 cDNA in healthy volunteers and Crohn's disease patients and identified two novel variants: a serine 138-to-glycine (S138G) and a glycine 330-to-arginine (G330R) substitution.0.0010857672003IL10RA11117998955AG
rs2241361743575622891ZNF365umls:C0010346GAD[Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.]0.1373835492007NA1062710915CT
rs224136192625234689NCF4umls:C0010346BeFreers224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.0.1285441822009NA1062710915CT
rs224136192625238929PHOX2Bumls:C0010346BeFreers224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.0.1281868632009NA1062710915CT
rs22413619262523339145FAM92Bumls:C0010346BeFreers224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.0.125548392009NA1062710915CT
rs2241432548996029761USP25umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0026384742015NA1062718076GA
rs224143254899605771PTPN2umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2690232122015NA1062718076GA
rs2241432548996022891ZNF365umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1373835492015NA1062718076GA
rs22414325489960159296NKX2-3umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2743860362015NA1062718076GA
rs2241432548996057178ZMIZ1umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1250055062015NA1062718076GA
rs224143254899602859GPR35umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0002714422015NA1062718076GA
rs22418791816208555054ATG16L1umls:C0010346BeFreeThe ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.0.3678631532008ATG16L1;SCARNA52233274822GA
rs224188020082483149233IL23Rumls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3705974352010ATG16L1;SCARNA52233274722AG
rs22418801789484955054ATG16L1umls:C0010346BeFreeIL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand Caucasians with inflammatory bowel disease.0.3678631532007ATG16L1;SCARNA52233274722AG
rs22418802515971055054ATG16L1umls:C0010346BeFreeHowever a possible role of ATG16L1 (T300A) on CD phenotype was suggested.0.3678631532014ATG16L1;SCARNA52233274722AG
rs22418802241238855054ATG16L1umls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.3678631532012ATG16L1;SCARNA52233274722AG
rs224188020066736149233IL23Rumls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.3705974352010ATG16L1;SCARNA52233274722AG
rs22418801965980855054ATG16L1umls:C0010346BeFreeGenome-wide association studies have described an association of the ATG16L1 (autophagy 16-like 1) gene rs2241880 variant with Crohn's disease (CD).0.3678631532009ATG16L1;SCARNA52233274722AG
rs2241880187155156584SLC22A5umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.0796694742008ATG16L1;SCARNA52233274722AG
rs2241880245222663593IL12Bumls:C0010346BeFreeDetection of Mycobacterium avium subspecies paratuberculosis in patients with Crohn's disease is unrelated to the presence of single nucleotide polymorphisms rs2241880 (ATG16L1) and rs10045431 (IL12B).0.1448320322014ATG16L1;SCARNA52233274722AG
rs22418802452226655054ATG16L1umls:C0010346BeFreeDetection of Mycobacterium avium subspecies paratuberculosis in patients with Crohn's disease is unrelated to the presence of single nucleotide polymorphisms rs2241880 (ATG16L1) and rs10045431 (IL12B).0.3678631532014ATG16L1;SCARNA52233274722AG
rs224188019491842345611IRGMumls:C0010346BeFreeThe aim of this study was to determine the role of the ATG16L1 (rs2241880) and IRGM (rs13361189 and rs4958847) genes polymorphism in Crohn's disease (CD) and ulcerative colitis (UC).0.170269082009ATG16L1;SCARNA52233274722AG
rs22418802006673655054ATG16L1umls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.3678631532010ATG16L1;SCARNA52233274722AG
rs22418801871551564127NOD2umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.562008ATG16L1;SCARNA52233274722AG
rs22418801720066964127NOD2umls:C0010346BeFreeWe found a statistically significant interaction with respect to Crohn disease risk between rs2241880 and the established CARD15 susceptibility variants (P = 0.039).0.562007ATG16L1;SCARNA52233274722AG
rs22418802006673664127NOD2umls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.562010ATG16L1;SCARNA52233274722AG
rs22418801871551555054ATG16L1umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.3678631532008ATG16L1;SCARNA52233274722AG
rs22418802022217155054ATG16L1umls:C0010346BeFreePublications addressing the relationship between rs2241880/T300A polymorphism of ATG16L1 and Crohn's disease (CD) and ulcerative colitis (UC) were selected from the MEDLINE and EMBASE databases.0.3678631532010ATG16L1;SCARNA52233274722AG
rs22418801949184255054ATG16L1umls:C0010346BeFreeThe aim of this study was to determine the role of the ATG16L1 (rs2241880) and IRGM (rs13361189 and rs4958847) genes polymorphism in Crohn's disease (CD) and ulcerative colitis (UC).0.3678631532009ATG16L1;SCARNA52233274722AG
rs224188017894849149233IL23Rumls:C0010346BeFreeIL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand Caucasians with inflammatory bowel disease.0.3705974352007ATG16L1;SCARNA52233274722AG
rs22418802008248355054ATG16L1umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.3678631532010ATG16L1;SCARNA52233274722AG
rs22418801957536155054ATG16L1umls:C0010346BeFreeThr300Ala polymorphism in ATG16L1 was reported as a susceptibility factor to Crohn's disease (CD).0.3678631532009ATG16L1;SCARNA52233274722AG
rs22418802008248364127NOD2umls:C0010346BeFreeOne hundred and eighty unrelated IBD patients [57 Crohn's disease (CD) and 123 ulcerative colitis (UC)] and 186 healthy controls were genotyped for the following known genetic susceptibility variants: NOD2 - Arg702Trp (rs2066844), Gly908Arg (rs2066845) and Leu1007insC (rs2066847), as well as IL23R - Arg381Gln (rs11209026) and ATG16L1 - Thr300Ala (rs2241880).0.562010ATG16L1;SCARNA52233274722AG
rs22418801816208555054ATG16L1umls:C0010346BeFreeThe ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.0.3678631532008ATG16L1;SCARNA52233274722AG
rs224188022412388677775SCARNA5umls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.122012ATG16L1;SCARNA52233274722AG
rs224188017435756677775SCARNA5umls:C0010346GWASCATGenome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.0.122007ATG16L1;SCARNA52233274722AG
rs22418802006673650941IBD5umls:C0010346BeFreeTo investigate the interaction of interleukin-23 receptor (IL23R) (rs1004819 and rs2201841), autophagy-related 16-like 1 (ATG16L1) (rs2241880), caspase recruitment domain-containing protein 15 (CARD15) genes, and IBD5 locus in Crohn's disease (CD) patients.0.0496165762010ATG16L1;SCARNA52233274722AG
rs22418801933775655054ATG16L1umls:C0010346BeFreeATG16L1 T300A polymorphism and Crohn's disease susceptibility: evidence from 13,022 cases and 17,532 controls.0.3678631532009ATG16L1;SCARNA52233274722AG
rs22418802402264255054ATG16L1umls:C0010346BeFreeT300A variant of autophagy ATG16L1 gene is associated with decreased antigen sampling and processing by dendritic cells in pediatric Crohn's disease.0.3678631532014ATG16L1;SCARNA52233274722AG
rs2241880187155156583SLC22A4umls:C0010346BeFreeWe confirmed a strong association between three NOD2/CARD15 gene variants (Pro268Ser, OR = 2.52, 95% CI = 1.34-4.75); (Arg702Trp, OR = 6.65, 95% CI = 1.99-22.17); (1007fs, OR = 9.59, 95% CI = 3.94-23.29), and a weak association between both the protective OCTN1/OCTN2 CC haplotype (OR = 0.28, 95% CI = 0.08-0.94), and a variant of ATG16L1 gene (Thr300Ala, OR = 0.468, 95% CI = 0.24-0.90) with Crohn's disease.0.0796595422008ATG16L1;SCARNA52233274722AG
rs22418801743575655054ATG16L1umls:C0010346GWASCATGenome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.0.3678631532007ATG16L1;SCARNA52233274722AG
rs2249296255579509635CLCA2umls:C0010346GWASCATIdentification of risk loci for Crohn's disease phenotypes using a genome-wide association study.0.122014CLCA2186444581TC
rs22749101858739455600ITLN1umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.1298254462008ITLN11160882256TC
rs22749101858739455600ITLN1umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1298254462008ITLN11160882256TC
rs2275913247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014IL17A652186235GA
rs22759132477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014IL17A652186235GA
rs2275913247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014IL17A652186235GA
rs2275913247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014IL17A652186235GA
rs2275913247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014IL17A652186235GA
rs2275913247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014IL17A652186235GA
rs2275913247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014IL17A652186235GA
rs2275913247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014IL17A652186235GA
rs2275913247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014IL17A652186235GA
rs2275913247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014IL17A652186235GA
rs22759132477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014IL17A652186235GA
rs2275913247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014IL17A652186235GA
rs2276707218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NR1I23119815306CG,T
rs22776801824877258191CXCL16umls:C0010346BeFreeIn this study, we demonstrate that in Crohn's disease (CD), the CXCL16 p.Ala181Val polymorphism is not a disease susceptibility gene but associated with younger age at disease onset (p=0.016) and higher frequency of ileal involvement (p=0.024; OR 2.17; 95% CI 1.12-4.21) in ValVal carriers compared to a higher frequency of colonic involvement in AlaAla carriers (p=0.009; OR 2.60; CI 1.29-5.25).0.0032672342008CXCL16174735268GA
rs2284553231282333460IFNGR2umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012IFNGR22133404389AG
rs23014362057096611116FGFR1OPumls:C0010346GWASCATFucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.0.1271010962010FGFR1OP6167024500CT
rs23014361858739411116FGFR1OPumls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1271010962008FGFR1OP6167024500CT
rs23014362057096611116FGFR1OPumls:C0010346GAD[Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.]0.1271010962010FGFR1OP6167024500CT
rs2301436185873941235CCR6umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0079154222008FGFR1OP6167024500CT
rs23014361858739411116FGFR1OPumls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.1271010962008FGFR1OP6167024500CT
rs2413583211024635155PDGFBumls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.0023670322010NA2239263768CT
rs2430561247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014IFNG1268158742TA
rs2430561247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014IFNG1268158742TA
rs2430561247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014IFNG1268158742TA
rs2430561247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014IFNG1268158742TA
rs24305612477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014IFNG1268158742TA
rs2430561247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014IFNG1268158742TA
rs24305612477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014IFNG1268158742TA
rs2430561247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014IFNG1268158742TA
rs2430561247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014IFNG1268158742TA
rs2430561247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014IFNG1268158742TA
rs2430561247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014IFNG1268158742TA
rs2430561247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014IFNG1268158742TA
rs2476601249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014PTPN22;AP4B1-AS11113834946AG
rs2476601249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014PTPN22;AP4B1-AS11113834946AG
rs24766012391397026191PTPN22umls:C0010346BeFreeOur data not only demonstrate a critical role of PTPN22 in regulating macrophage polarization but also provide a molecular explanation for the protective effect of the C1858T SNP in Crohn's disease.0.1537572762013PTPN22;AP4B1-AS11113834946AG
rs24766012497146126191PTPN22umls:C0010346BeFreeAfter Bonferroni correction for multiple testing, both the homozygous and the heterozygous variant genotypes of IL23R G>A(rs11209026) (OR(CD,adj): 0.38, 95% CI: 0.21-0.67, p = 0.03; OR(IBD,adj) 0.43, 95% CI: 0.28-0.67, p = 0.007) and PTPN22 1858 G>A(rs2476601) (OR(CD,unadj) 0.54, 95% CI: 0.41-0.72, p = 7*10-4; OR(IBD,unadj): 0.61, 95% CI: 0.48-0.77, p = 0.001) were associated with reduced risk of CD.0.1537572762014PTPN22;AP4B1-AS11113834946AG
rs24766011639155526191PTPN22umls:C0010346GAD[Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis.]0.1537572762006PTPN22;AP4B1-AS11113834946AG
rs24766012110246326191PTPN22umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1537572762010PTPN22;AP4B1-AS11113834946AG
rs24766011858739426191PTPN22umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.1537572762008PTPN22;AP4B1-AS11113834946AG
rs2476601249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014PTPN22;AP4B1-AS11113834946AG
rs247660124971461149233IL23Rumls:C0010346BeFreeAfter Bonferroni correction for multiple testing, both the homozygous and the heterozygous variant genotypes of IL23R G>A(rs11209026) (OR(CD,adj): 0.38, 95% CI: 0.21-0.67, p = 0.03; OR(IBD,adj) 0.43, 95% CI: 0.28-0.67, p = 0.007) and PTPN22 1858 G>A(rs2476601) (OR(CD,unadj) 0.54, 95% CI: 0.41-0.72, p = 7*10-4; OR(IBD,unadj): 0.61, 95% CI: 0.48-0.77, p = 0.001) were associated with reduced risk of CD.0.3705974352014PTPN22;AP4B1-AS11113834946AG
rs25421511755430056984PSMG2umls:C0010346GAD[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]0.0071010962007NA1812779948GT
rs25421511755426156984PSMG2umls:C0010346GAD[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]0.0071010962007NA1812779948GT
rs25421511858739456984PSMG2umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0071010962008NA1812779948GT
rs25497942110246364167ERAP2umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.2423670322010ERAP1;ERAP2596908845CT
rs25497942110246364167ERAP2umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.2423670322010ERAP1;ERAP2596908845CT
rs2569190247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014CD14;TMCO65140633331AG
rs2569190247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014CD14;TMCO65140633331AG
rs2569190247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014CD14;TMCO65140633331AG
rs2569190247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014CD14;TMCO65140633331AG
rs2569190247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014CD14;TMCO65140633331AG
rs25691902477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014CD14;TMCO65140633331AG
rs25691902477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014CD14;TMCO65140633331AG
rs2569190247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014CD14;TMCO65140633331AG
rs2569190247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014CD14;TMCO65140633331AG
rs2569190247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014CD14;TMCO65140633331AG
rs2569190247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014CD14;TMCO65140633331AG
rs2569190247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014CD14;TMCO65140633331AG
rs2631367163613056584SLC22A5umls:C0010346BeFreeGenetic association between Crohn's disease (CD) and OCTN1 (SLC22A4) C1672T/OCTN2 (SLC22A5) G-207C variants in IBD5 has recently been reported.0.0796694742006SLC22A5;LOC5531035132369766CG
rs2631367163613056583SLC22A4umls:C0010346BeFreeGenetic association between Crohn's disease (CD) and OCTN1 (SLC22A4) C1672T/OCTN2 (SLC22A5) G-207C variants in IBD5 has recently been reported.0.0796595422006SLC22A5;LOC5531035132369766CG
rs2631367212797236583SLC22A4umls:C0010346BeFreeTo evaluate the association of the IBD5 locus to the predisposition of inflammatory bowel diseases (IBDs), a series of meta-analyses between five IBD5 variants (OCTN1 C1672T, OCTN2 G-207C, OCTN1/2 TC haplotype, IGR2096a_1, IGR2198a_1 and IGR2230a_1) and Crohn's disease (CD) and ulcerative colitis (UC) were performed, which included a total of 26 studies.0.0796595422011SLC22A5;LOC5531035132369766CG
rs2631367173915616583SLC22A4umls:C0010346BeFreePlasma carnitine ester profiles in Crohn's disease patients characterized for SLC22A4 C1672T and SLC22A5 G-207C genotypes.0.0796595422007SLC22A5;LOC5531035132369766CG
rs2631367173915616584SLC22A5umls:C0010346BeFreePlasma carnitine ester profiles in Crohn's disease patients characterized for SLC22A4 C1672T and SLC22A5 G-207C genotypes.0.0796694742007SLC22A5;LOC5531035132369766CG
rs26313671636130550941IBD5umls:C0010346BeFreeGenetic association between Crohn's disease (CD) and OCTN1 (SLC22A4) C1672T/OCTN2 (SLC22A5) G-207C variants in IBD5 has recently been reported.0.0496165762006SLC22A5;LOC5531035132369766CG
rs2631367212797236584SLC22A5umls:C0010346BeFreeTo evaluate the association of the IBD5 locus to the predisposition of inflammatory bowel diseases (IBDs), a series of meta-analyses between five IBD5 variants (OCTN1 C1672T, OCTN2 G-207C, OCTN1/2 TC haplotype, IGR2096a_1, IGR2198a_1 and IGR2230a_1) and Crohn's disease (CD) and ulcerative colitis (UC) were performed, which included a total of 26 studies.0.0796694742011SLC22A5;LOC5531035132369766CG
rs26313672127972350941IBD5umls:C0010346BeFreeTo evaluate the association of the IBD5 locus to the predisposition of inflammatory bowel diseases (IBDs), a series of meta-analyses between five IBD5 variants (OCTN1 C1672T, OCTN2 G-207C, OCTN1/2 TC haplotype, IGR2096a_1, IGR2198a_1 and IGR2230a_1) and Crohn's disease (CD) and ulcerative colitis (UC) were performed, which included a total of 26 studies.0.0496165762011SLC22A5;LOC5531035132369766CG
rs2695121212459924790NFKB1umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0082628082011NR1H21950377484TC
rs2695121212459928856NR1I2umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0069914752011NR1H21950377484TC
rs2797685211024638863PER3umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1223670322010PER317819003CT
rs2797685211024638863PER3umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1223670322010PER317819003CT
rs28232562548996029761USP25umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0026384742015LOC1019277452115412387GA
rs2823256254899605771PTPN2umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2690232122015LOC1019277452115412387GA
rs28232562548996057178ZMIZ1umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1250055062015LOC1019277452115412387GA
rs28232562548996022891ZNF365umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1373835492015LOC1019277452115412387GA
rs2823256254899602859GPR35umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0002714422015LOC1019277452115412387GA
rs282325625489960159296NKX2-3umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2743860362015LOC1019277452115412387GA
rs2834215229366693460IFNGR2umls:C0010346GWASCATWe also found suggestive evidence for the association of the IFNGR2 (21q22.11), FOXP2 (7q31), MACROD2 (20p12.1) and AIF1 (6p21.3) loci with CD risk.0.122013IFNGR22133424579AG
rs28360457172572215027P2RX7umls:C0010346BeFreeFunctional P2X7 receptor polymorphisms (His155Tyr, Arg307Gln, Glu496Ala) in patients with Crohn's disease.0.0008143262007P2RX7;LOC10537003212121175426GA
rs28362491249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014NFKB1;LOC1053776214102500998ATTG-
rs28362491249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014NFKB1;LOC1053776214102500998ATTG-
rs28362491212459928856NR1I2umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0069914752011NFKB1;LOC1053776214102500998ATTG-
rs28362491212459924790NFKB1umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0082628082011NFKB1;LOC1053776214102500998ATTG-
rs28362491249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014NFKB1;LOC1053776214102500998ATTG-
rs2838519211024638209C21orf33umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1223670322010LOC1053771392144195140GA
rs287250718587394124626ZPBP2umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0023670322008NA1739884510GA
rs28725071858739494103ORMDL3umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0052769482008NA1739884510GA
rs28725072269493055876GSDMBumls:C0010346BeFreeThe minor allele A of rs2872507 in GSDMB is the protective allele for asthma but the risk allele for rheumatoid arthritis, Crohn disease, and ulcerative colitis.0.0073725382012NA1739884510GA
rs290244017804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167205233GA
rs2945412231282338844KSR1umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012KSR11727516617GA
rs3024505205098893586IL10umls:C0010346GAD[The polymorphism rs3024505 proximal to IL-10 is associated with risk of ulcerative colitis and Crohns disease in a Danish case-control study.]0.1655250852010NA1206766559GA
rs3024505249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014NA1206766559GA
rs3024505205098893586IL10umls:C0010346BeFreeThe polymorphism rs3024505 proximal to IL-10 is associated with risk of ulcerative colitis and Crohns disease in a Danish case-control study.0.1655250852010NA1206766559GA
rs3024505249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014NA1206766559GA
rs3024505249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014NA1206766559GA
rs3091315211024636347CCL2umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1355594012010NA1734266646AG
rs3091316224123886347CCL2umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.1355594012012NA1734266955GA
rs3091338224123883562IL3umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.0023670322012NA5132067045CT
rs309418823266558100130889PSORS1C3umls:C0010346GWASCATA genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.0.122013PSORS1C3631174468CA
rs3135932127594363587IL10RAumls:C0010346BeFreeWe decided to screen for mutations of the IL-10R1 cDNA in healthy volunteers and Crohn's disease patients and identified two novel variants: a serine 138-to-glycine (S138G) and a glycine 330-to-arginine (G330R) substitution.0.0010857672003IL10RA11117993348AG
rs31800182110246310067SCAMP3umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1223670322010NANANANANA
rs3197999185873944485MST1umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.2558308432008MST1349684099GA
rs3197999211024634485MST1umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.2558308432010MST1349684099GA
rs3197999185873944485MST1umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.2558308432008MST1349684099GA
rs3197999220872774485MST1umls:C0010346BeFreeProtein characterization of a candidate mechanism SNP for Crohn's disease: the macrophage stimulating protein R689C substitution.0.2558308432011MST1349684099GA
rs324420190539812166FAAHumls:C0010346BeFreeTo analyse FAAH expression and the FAAH 385 C/A (p.Pro129Thr; rs324420) single nucleotide polymorphism (SNP) in-patients with Crohn's disease (CD) and ulcerative colitis (UC).0.0029099162009FAAH146405089CA
rs324420184937292166FAAHumls:C0010346BeFreeGenomic DNA from 202 patients with Crohn's disease (CD) and 206 healthy controls was analyzed for the C385A polymorphism in the FAAH gene to address a possible role in humans.0.0029099162008FAAH146405089CA
rs352139247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014TLR9352224356TC
rs352139247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014TLR9352224356TC
rs352139247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014TLR9352224356TC
rs352139247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014TLR9352224356TC
rs3521392477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014TLR9352224356TC
rs3521392477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR9352224356TC
rs352139247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014TLR9352224356TC
rs352139247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014TLR9352224356TC
rs352139249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014TLR9352224356TC
rs352139249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014TLR9352224356TC
rs352139247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR9352224356TC
rs352139247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014TLR9352224356TC
rs352139247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014TLR9352224356TC
rs352139247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014TLR9352224356TC
rs352139249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014TLR9352224356TC
rs358294192018245122900CARD8umls:C0010346BeFreeEvidence of interaction of CARD8 rs2043211 with NALP3 rs35829419 in Crohn's disease.0.0085441822010NLRP31247425556CA
rs3582941920182451114548NLRP3umls:C0010346GAD[Evidence of interaction of CARD8 rs2043211 with NALP3 rs35829419 in Crohn's disease.]0.1408126052010NLRP31247425556CA
rs3582941920182451114548NLRP3umls:C0010346BeFreeEvidence of interaction of CARD8 rs2043211 with NALP3 rs35829419 in Crohn's disease.0.1408126052010NLRP31247425556CA
rs358294192018245164127NOD2umls:C0010346BeFreeWe found that the presence of the minor allele of rs2043211 with the major allele of rs35829419 conferred a protective effect against Crohn's disease (and vice versa), which intensified in the absence of NOD2 mutations (P(1,2/1,1)=0.009, odds ratio (OR)=0.66, 95% confidence interval (CI) (0.48-0.90); P(1,1/1,2)=0.015, OR=0.35, 95% CI (0.15-0.82)).0.562010NLRP31247425556CA
rs35873774187753087495XBP1P1umls:C0010346BeFreeAn association of XBP1 variants with both forms of human IBD (Crohn's disease and ulcerative colitis) was identified and replicated (rs35873774; p value 1.6 x 10(-5)) with novel, private hypomorphic variants identified as susceptibility factors.0.0010857672008XBP12228795944AG
rs3594572110246391272BOD1umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.0023670322010NA5173852839CT
rs361525247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014TNF631575324GA
rs361525247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014TNF631575324GA
rs3615252477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TNF631575324GA
rs361525247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014TNF631575324GA
rs361525247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014TNF631575324GA
rs361525247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014TNF631575324GA
rs361525247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014TNF631575324GA
rs361525247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014TNF631575324GA
rs361525247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TNF631575324GA
rs361525247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014TNF631575324GA
rs3615252477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014TNF631575324GA
rs361525247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014TNF631575324GA
rs3712099852370915764127NOD2umls:C0010346BeFreeThree common NOD2 mutations are associated with Crohn's disease (p=5.08×10(-7), 1.67×10(-6), and 1.87×10(-2) for 1007fs, R720W, and G908R, respectively), but not with ulcerative colitis (p=0.1046, 0.1269, and 0.8929, respectively).0.562013WDHD11454957612CT
rs3732378164055401524CX3CR1umls:C0010346BeFreeIncreased expression of the chemokine fractalkine in Crohn's disease and association of the fractalkine receptor T280M polymorphism with a fibrostenosing disease Phenotype.0.0059057082006CX3CR1339265671GA
rs37323781861777964127NOD2umls:C0010346BeFreeOur aim was to evaluate the frequency of CX3CR1 V249I and T280M polymorphisms and NOD2/CARD15 mutations in Crohn's disease patients and to search for a relationship with phenotype.0.562008CX3CR1339265671GA
rs3732379186177791524CX3CR1umls:C0010346BeFreeThe V249I polymorphism of the CX3CR1 gene is associated with fibrostenotic disease behavior in patients with Crohn's disease.0.0059057082008CX3CR1339265765CT
rs37323791861777964127NOD2umls:C0010346BeFreeOur aim was to evaluate the frequency of CX3CR1 V249I and T280M polymorphisms and NOD2/CARD15 mutations in Crohn's disease patients and to search for a relationship with phenotype.0.562008CX3CR1339265765CT
rs3749172254899605771PTPN2umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2690232122015GPR352240630832AC,T
rs37491722548996029761USP25umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0026384742015GPR352240630832AC,T
rs37491722548996022891ZNF365umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1373835492015GPR352240630832AC,T
rs374917225489960159296NKX2-3umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2743860362015GPR352240630832AC,T
rs37491722548996057178ZMIZ1umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1250055062015GPR352240630832AC,T
rs3749172254899602859GPR35umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0002714422015GPR352240630832AC,T
rs3751143172572215027P2RX7umls:C0010346BeFreeFunctional P2X7 receptor polymorphisms (His155Tyr, Arg307Gln, Glu496Ala) in patients with Crohn's disease.0.0008143262007P2RX7;LOC10537003212121184501AC
rs37637722818088064149233IL23Rumls:C0010346BeFreeGiven the association of IL23R with inflammatory bowel disease (IBD), we characterized the role of IL-17F in IBD including its intestinal gene expression and the effect of the IL17F p.His161Arg polymorphism on disease susceptibility and phenotype of Crohn's disease (CD) and ulcerative colitis (UC).0.3705974352008IL23R167182950AG
rs376414718587394144811LACC1umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.129739572008LACC11343883789AG
rs376414718587394144811LACC1umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.129739572008LACC11343883789AG
rs376414721102463144811LACC1umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.129739572010LACC11343883789AG
rs376414723128233144811LACC1umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.129739572012LACC11343883789AG
rs379210922936669677775SCARNA5umls:C0010346GWASCATA genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.0.122013ATG16L1;SCARNA52233275771GA
rs37921092110246355054ATG16L1umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.3678631532010ATG16L1;SCARNA52233275771GA
rs379210921102463677775SCARNA5umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.122010ATG16L1;SCARNA52233275771GA
rs37921092293666955054ATG16L1umls:C0010346GWASCATA genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.0.3678631532013ATG16L1;SCARNA52233275771GA
rs3792876174766806583SLC22A4umls:C0010346GAD[Polymorphisms 3020insC in CARD15 and SNP rs3792876 in SLC22A4/5 occurred statistically significantly more often in patients with pediatric-onset CD than in patients with adult-onset CD. Polymorphisms 3020insC in CARD15 and SNP rs2165047 in DLG5 were assoc]0.0796595422007SLC22A45132301616CT
rs3792876174766806584SLC22A5umls:C0010346GAD[Polymorphisms 3020insC in CARD15 and SNP rs3792876 in SLC22A4/5 occurred statistically significantly more often in patients with pediatric-onset CD than in patients with adult-onset CD. Polymorphisms 3020insC in CARD15 and SNP rs2165047 in DLG5 were assoc]0.0796694742007SLC22A45132301616CT
rs3804099247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014TLR24153703504TC
rs3804099247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR24153703504TC
rs3804099247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014TLR24153703504TC
rs3804099247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014TLR24153703504TC
rs3804099247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014TLR24153703504TC
rs3804099247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014TLR24153703504TC
rs3804099247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014TLR24153703504TC
rs3804099247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014TLR24153703504TC
rs3804099247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014TLR24153703504TC
rs38040992477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014TLR24153703504TC
rs38040992477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR24153703504TC
rs3804099247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014TLR24153703504TC
rs3810936211024639966TNFSF15umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1648303112010TNFSF159114790605TC
rs3814055218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NR1I23119781188CT
rs3814057218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NR1I23119818407AC
rs38283091858739455054ATG16L1umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.3678631532008ATG16L12233271764AG
rs3865136442019548056144PCDHA4umls:C0010346BeFreeThe cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's disease.0.0002714422010NANANANANA
rs386525803218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NANANANANA
rs386599677235934637100TLR5umls:C0010346BeFreeA non-synonymous coding variant (L616F) in the TLR5 gene is potentially associated with Crohn's disease and influences responses to bacterial flagellin.0.0035386762013NANANANANA
rs393650319174780219771CCNYumls:C0010346GAD[Confirmation of multiple Crohn's disease susceptibility loci in a large Dutch-Belgian cohort.]0.2569265422009CCNY1035260329GA
rs40775152110246364170CARD9umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1250055062010CARD99136372044CT
rs40775152110246364170CARD9umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1250055062010CARD99136372044CT
rs4149570249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014TNFRSF1A126342424AC
rs4149570247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014TNFRSF1A126342424AC
rs4149570247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014TNFRSF1A126342424AC
rs4149570247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014TNFRSF1A126342424AC
rs4149570249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014TNFRSF1A126342424AC
rs41495702477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TNFRSF1A126342424AC
rs4149570247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014TNFRSF1A126342424AC
rs4149570247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014TNFRSF1A126342424AC
rs41495702477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014TNFRSF1A126342424AC
rs4149570247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014TNFRSF1A126342424AC
rs4149570247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014TNFRSF1A126342424AC
rs4149570247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014TNFRSF1A126342424AC
rs4149570247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014TNFRSF1A126342424AC
rs4149570247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TNFRSF1A126342424AC
rs4149570249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014TNFRSF1A126342424AC
rs4251961247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014IL1RN2113116890TC
rs4251961247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014IL1RN2113116890TC
rs4251961247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014IL1RN2113116890TC
rs4251961247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014IL1RN2113116890TC
rs4251961247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014IL1RN2113116890TC
rs4251961247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014IL1RN2113116890TC
rs42519612477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014IL1RN2113116890TC
rs4251961247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014IL1RN2113116890TC
rs4251961247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014IL1RN2113116890TC
rs4251961247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014IL1RN2113116890TC
rs42519612477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014IL1RN2113116890TC
rs4251961247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014IL1RN2113116890TC
rs4263839216366469966TNFSF15umls:C0010346BeFreeThe Crohn's disease risk allele rs4263839 G in the TNFSF15 gene was significantly associated with an increased risk of both IBS (p=2.2×10(-5); OR 1.37) and more pronouncedly, IBS-C (p=8.7×10(-7); OR 1.79) in the entire sample.0.1648303112011TNFSF159114804160AG
rs4263839185873949966TNFSF15umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.1648303112008TNFSF159114804160AG
rs44097642548996022891ZNF365umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1373835492015NA1099524480TG
rs4409764254899602859GPR35umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0002714422015NA1099524480TG
rs44097642548996057178ZMIZ1umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1250055062015NA1099524480TG
rs44097642548996029761USP25umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0026384742015NA1099524480TG
rs4409764211024632805GOT1umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.0073725382010NA1099524480TG
rs4409764254899605771PTPN2umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2690232122015NA1099524480TG
rs440976425489960159296NKX2-3umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2743860362015NA1099524480TG
rs4411591247071447124TNFumls:C0010346BeFreeAssociation of rs1568885, rs1813443 and rs4411591 polymorphisms with anti-TNF medication response in Greek patients with Crohn's disease.0.4222949572014LINC01387186550118CT
rs4537545249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014IL6R1154446403CT
rs4537545249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014IL6R1154446403CT
rs4537545249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014IL6R1154446403CT
rs45610735218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NANANANANA
rs4613763185873941601DAB2umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0165692242008NA540392626TC
rs4613763185873945734PTGER4umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0185551932008NA540392626TC
rs46569402110246351744CD244umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.122010CD2441160860478AG
rs4696480247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014TLR24153685974TA
rs4696480247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014TLR24153685974TA
rs4696480247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014TLR24153685974TA
rs4696480247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014TLR24153685974TA
rs4696480247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014TLR24153685974TA
rs46964802477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR24153685974TA
rs4696480247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR24153685974TA
rs4696480247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014TLR24153685974TA
rs4696480247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014TLR24153685974TA
rs4696480247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014TLR24153685974TA
rs46964802477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014TLR24153685974TA
rs4696480247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014TLR24153685974TA
rs4780355224828048651SOCS1umls:C0010346GWASCATIn addition, we identified one susceptibility locus for CD (16p13 near SOCS1, p(rs4780355) = 4.99 × 10(-8)).0.122012SOCS1;LOC1053710821611254001TC
rs4802307231282335536PPP5Cumls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012PPP5C1946346549GT
rs48048031807033630835CD209umls:C0010346BeFreeA functional variant in the CD209 gene, rs4804803, does not seem to be influencing Crohn's disease susceptibility.0.0053628242007CD209197747847AG
rs48093302110246384619ZGPATumls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1271010962010ZGPAT2063718234AG
rs48093302110246384619ZGPATumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1271010962010ZGPAT2063718234AG
rs4848306247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014NA2112840530GA
rs4848306247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014NA2112840530GA
rs48483062477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014NA2112840530GA
rs4848306247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014NA2112840530GA
rs4848306247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014NA2112840530GA
rs4848306247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014NA2112840530GA
rs4848306247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014NA2112840530GA
rs4848306247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014NA2112840530GA
rs4848306247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014NA2112840530GA
rs4848306247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014NA2112840530GA
rs4848306247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014NA2112840530GA
rs48483062477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014NA2112840530GA
rs49588471949184255054ATG16L1umls:C0010346BeFreeThe aim of this study was to determine the role of the ATG16L1 (rs2241880) and IRGM (rs13361189 and rs4958847) genes polymorphism in Crohn's disease (CD) and ulcerative colitis (UC).0.3678631532009IRGM5150860025GA
rs495884719491842345611IRGMumls:C0010346BeFreeThe aim of this study was to determine the role of the ATG16L1 (rs2241880) and IRGM (rs13361189 and rs4958847) genes polymorphism in Crohn's disease (CD) and ulcerative colitis (UC).0.170269082009IRGM5150860025GA
rs49867901868022364127NOD2umls:C0010346BeFreeTo evaluate the role of genetic factors in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC), we investigated the single nucleotide polymorphisms (SNPs) of NOD2/CARD15 (R702W, G908R and L1007finsC), and Toll-like receptor 4 (TLR4) genes (D299G and T399I) in a selected inflammatory bowel disease (IBD) population coming from Southern Italy.0.562008TLR49117713024AG
rs4986790200938347099TLR4umls:C0010346BeFreeThe Toll-like receptor 4 D299G and T399I polymorphisms are associated with Crohn's disease and ulcerative colitis: a meta-analysis.0.1828426212010TLR49117713024AG
rs4986790178504117099TLR4umls:C0010346BeFreeThe TLR4 Asp299Gly and Thr399Ile polymorphisms were genotyped and tested for case-control frequency differences in a New Zealand white cohort of 389 Crohn's disease (CD) patients, 405 ulcerative colitis (UC) patients, and 416 population controls.0.1828426212007TLR49117713024AG
rs49867901597311864127NOD2umls:C0010346BeFreeThe role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease.0.562005TLR49117713024AG
rs4986790159731187099TLR4umls:C0010346BeFreeThe role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease.0.1828426212005TLR49117713024AG
rs4986790181746807099TLR4umls:C0010346BeFreeIn this two-center, retrospective German and Hungarian cohort study, patients with Crohn's disease (CD) (n = 379; German n = 235, Hungarian n = 144) and ulcerative colitis (UC) (n = 263; German n = 145, Hungarian n = 118) and healthy controls (n = 605; German n = 403, Hungarian n = 202) were genotyped for the presence of the CD14 c.1-260C>T promoter variant and the TLR4 c.896A>G (p.D299G) variant by melting curve analysis using fluorescence resonance energy transfer probes.0.1828426212007TLR49117713024AG
rs4986790229186827099TLR4umls:C0010346BeFreeToll-like receptor (TLR) polymorphisms, and especially TLR-4 Asp299Gly and TLR-4 Thr399Ile, have been linked with Crohn's disease (CD) and to a lesser extent with ulcerative colitis (UC), CD behavior, and compromised seroreactivity to microbial antigens.0.1828426212013TLR49117713024AG
rs4986790184932107099TLR4umls:C0010346BeFreeTo examine whether TLR4 Asp299Gly, CD14-260C/T, TNF-1031T/C, TNF-863C/A, TNF-857C/T, TACE-172C/T, and TACE-154C/A polymorphisms are associated with Crohn disease in the Ashkenazi Jewish population, we analyzed families with at least 1 child with Crohn disease for association with these mutations using a family-based association test (transmission disequilibrium test) for analysis.0.1828426212008TLR49117713024AG
rs498679018174680929CD14umls:C0010346BeFreeIn this two-center, retrospective German and Hungarian cohort study, patients with Crohn's disease (CD) (n = 379; German n = 235, Hungarian n = 144) and ulcerative colitis (UC) (n = 263; German n = 145, Hungarian n = 118) and healthy controls (n = 605; German n = 403, Hungarian n = 202) were genotyped for the presence of the CD14 c.1-260C>T promoter variant and the TLR4 c.896A>G (p.D299G) variant by melting curve analysis using fluorescence resonance energy transfer probes.0.0310950582007TLR49117713024AG
rs4986790184932106868ADAM17umls:C0010346BeFreeTo examine whether TLR4 Asp299Gly, CD14-260C/T, TNF-1031T/C, TNF-863C/A, TNF-857C/T, TACE-172C/T, and TACE-154C/A polymorphisms are associated with Crohn disease in the Ashkenazi Jewish population, we analyzed families with at least 1 child with Crohn disease for association with these mutations using a family-based association test (transmission disequilibrium test) for analysis.0.0029099162008TLR49117713024AG
rs4986790181746804695NDUFA2umls:C0010346BeFreeIn this two-center, retrospective German and Hungarian cohort study, patients with Crohn's disease (CD) (n = 379; German n = 235, Hungarian n = 144) and ulcerative colitis (UC) (n = 263; German n = 145, Hungarian n = 118) and healthy controls (n = 605; German n = 403, Hungarian n = 202) were genotyped for the presence of the CD14 c.1-260C>T promoter variant and the TLR4 c.896A>G (p.D299G) variant by melting curve analysis using fluorescence resonance energy transfer probes.0.0046145122007TLR49117713024AG
rs4986790182136977099TLR4umls:C0010346BeFreeNovel NOD2 haplotype strengthens the association between TLR4 Asp299gly and Crohn's disease in an Australian population.0.1828426212008TLR49117713024AG
rs4986790186802237099TLR4umls:C0010346BeFreeTo evaluate the role of genetic factors in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC), we investigated the single nucleotide polymorphisms (SNPs) of NOD2/CARD15 (R702W, G908R and L1007finsC), and Toll-like receptor 4 (TLR4) genes (D299G and T399I) in a selected inflammatory bowel disease (IBD) population coming from Southern Italy.0.1828426212008TLR49117713024AG
rs49867901821369764127NOD2umls:C0010346BeFreeNovel NOD2 haplotype strengthens the association between TLR4 Asp299gly and Crohn's disease in an Australian population.0.562008TLR49117713024AG
rs4986791159731187099TLR4umls:C0010346BeFreeThe role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease.0.1828426212005TLR49117713324CT
rs4986791229186827099TLR4umls:C0010346BeFreeToll-like receptor (TLR) polymorphisms, and especially TLR-4 Asp299Gly and TLR-4 Thr399Ile, have been linked with Crohn's disease (CD) and to a lesser extent with ulcerative colitis (UC), CD behavior, and compromised seroreactivity to microbial antigens.0.1828426212013TLR49117713324CT
rs4986791178504117099TLR4umls:C0010346BeFreeThe TLR4 Asp299Gly and Thr399Ile polymorphisms were genotyped and tested for case-control frequency differences in a New Zealand white cohort of 389 Crohn's disease (CD) patients, 405 ulcerative colitis (UC) patients, and 416 population controls.0.1828426212007TLR49117713324CT
rs49867911597311864127NOD2umls:C0010346BeFreeThe role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease.0.562005TLR49117713324CT
rs4986791186802237099TLR4umls:C0010346BeFreeTo evaluate the role of genetic factors in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC), we investigated the single nucleotide polymorphisms (SNPs) of NOD2/CARD15 (R702W, G908R and L1007finsC), and Toll-like receptor 4 (TLR4) genes (D299G and T399I) in a selected inflammatory bowel disease (IBD) population coming from Southern Italy.0.1828426212008TLR49117713324CT
rs49867911868022364127NOD2umls:C0010346BeFreeTo evaluate the role of genetic factors in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC), we investigated the single nucleotide polymorphisms (SNPs) of NOD2/CARD15 (R702W, G908R and L1007finsC), and Toll-like receptor 4 (TLR4) genes (D299G and T399I) in a selected inflammatory bowel disease (IBD) population coming from Southern Italy.0.562008TLR49117713324CT
rs4986791200938347099TLR4umls:C0010346BeFreeThe Toll-like receptor 4 D299G and T399I polymorphisms are associated with Crohn's disease and ulcerative colitis: a meta-analysis.0.1828426212010TLR49117713324CT
rs50307282477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR49117712004GA
rs5030728247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014TLR49117712004GA
rs5030728247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014TLR49117712004GA
rs5030728247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014TLR49117712004GA
rs5030728247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014TLR49117712004GA
rs5030728247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014TLR49117712004GA
rs50307282477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014TLR49117712004GA
rs5030728247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014TLR49117712004GA
rs5030728247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014TLR49117712004GA
rs5030728247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014TLR49117712004GA
rs5030728247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014TLR49117712004GA
rs5030728247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014TLR49117712004GA
rs504963205709662524FUT2umls:C0010346GWASCATFucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.0.2471770412010FUT2;LOC1054476451948705608GA
rs514000254899605771PTPN2umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2690232122015PTPN21812854073CT
rs514000254899602859GPR35umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0002714422015PTPN21812854073CT
rs5140002548996057178ZMIZ1umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1250055062015PTPN21812854073CT
rs5140002548996022891ZNF365umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.1373835492015PTPN21812854073CT
rs5140002548996029761USP25umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.0026384742015PTPN21812854073CT
rs51400025489960159296NKX2-3umls:C0010346BeFreeWe confirmed 6 previously reported loci in Caucasian: GPR35 at 2q37 (rs3749172; P = 5.30 × 10, odds ratio [OR] = 1.45), ZNF365 at 10q21 (rs224143; P = 2.20 × 10, OR = 1.38), ZMIZ1 at 10q22 (rs1250569; P = 3.05 × 10, OR = 1.30), NKX2-3 at 10q24 (rs4409764; P = 7.93 × 10, OR = 1.32), PTPN2 at 18p11 (rs514000; P = 9.00 × 10, OR = 1.33), and USP25 at 21q11 (rs2823256; P = 2.49 × 10, OR = 1.35), bringing the number of known CD loci (including 3 in the HLA) in Koreans to 15.0.2743860362015PTPN21812854073CT
rs516246231282332524FUT2umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.2471770412012FUT2;LOC1054476451948702915CT
rs57432891744784264127NOD2umls:C0010346GWASCATTwo of these (IL23R on Chromosome 1 and CARD15 on Chromosome 16) correspond to genes previously reported to be associated with CD.0.562007NOD21650722863CG,T
rs57432891780478964127NOD2umls:C0010346GWASCATA proportion of these were replicated in two independent German Caucasian samples, including the established CD loci NOD2 and IBD5.0.562007NOD21650722863CG,T
rs57432931957005264127NOD2umls:C0010346BeFreeNOD2/CARD15 is involved in the innate immune response and three polymorphisms in this gene (Arg702Trp rs2066844, Gly908Arg rs2066845 and Leu1007fsinsC rs5743293) have been associated with risk of the rare Crohn's disease.0.562010NOD21650729870-C
rs5744174235934637100TLR5umls:C0010346BeFreeA non-synonymous coding variant (L616F) in the TLR5 gene is potentially associated with Crohn's disease and influences responses to bacterial flagellin.0.0035386762013TLR51223111186AG
rs60872763212510661493CTLA4umls:C0010346BeFreeAssociation of cytotoxic T lymphocyte associated antigen-4 gene (rs60872763) polymorphism with Crohn's disease and high levels of serum sCTLA-4 in Crohn's disease.0.0146354552011CTLA42203873378ATATAT-
rs6478106232665583133HLA-Eumls:C0010346BeFreeWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.0016286512013NA9114783386CT
rs6478106232665589966TNFSF15umls:C0010346BeFreeWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.1648303112013NA9114783386CT
rs6478106232665586774STAT3umls:C0010346BeFreeWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.1461892422013NA9114783386CT
rs654594622412388200728TMEM17umls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.122012TMEM17262486398CT
rs65459462241238810678B3GNT2umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.0023670322012TMEM17262486398CT
rs655641221102463285626LOC285626umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.122010LOC2856265159360377GA
rs6601764175543001316KLF6umls:C0010346GAD[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]0.0023670322007NA103820350CT
rs66796772312823310745PHTF1umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012PHTF11113761186CA
rs67167532312823311262SP140umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.1223670322012SP1402230232414TC
rs6738825211024635334PLCL1umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.0023670322010PLCL12198032171AG
rs6785049218302708856NR1I2umls:C0010346BeFreeGenomic DNA from 2823 individuals of Caucasian origin including 859 patients with Crohn's disease (CD), 464 patients with ulcerative colitis (UC), and 1500 healthy, unrelated controls was analyzed for eight PXR/NR1I2 single nucleotide polymorphisms (SNPs) (rs12721602 (-25564), rs3814055 (-25385), rs1523128 (-24756), rs1523127 (-24381), rs45610735 = p.Gly36Arg (+106), rs6785049 (+7635), rs2276707 (+8055), and rs3814057 (+11156)).0.0069914752011NR1I23119814886GA
rs68373352312823357606SLAIN2umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012SLAIN2448361966AG
rs6887695257611853593IL12Bumls:C0010346BeFreeOur genetic association study revealed that the polymorphisms of IL12B rs6887695 were associated with both CD and ulcerative colitis (UC) susceptibility in Chinese population, but did not affect the serum IL12p40 level in either CD patients or UC patients.0.1448320322015NA5159395637GC
rs6887695175542613593IL12Bumls:C0010346GAD[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]0.1448320322007NA5159395637GC
rs69084251858739454901CDKAL1umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.1365692242008CDKAL1620728500TC
rs69084252110246354901CDKAL1umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1365692242010CDKAL1620728500TC
rs69084251858739454901CDKAL1umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1365692242008CDKAL1620728500TC
rs6927172247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014NA6137681038CG
rs69271722477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014NA6137681038CG
rs6927172247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014NA6137681038CG
rs6927172247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014NA6137681038CG
rs6927172247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014NA6137681038CG
rs6927172247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014NA6137681038CG
rs6927172247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014NA6137681038CG
rs6927172247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014NA6137681038CG
rs6927172247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014NA6137681038CG
rs6927172247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014NA6137681038CG
rs69271722477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014NA6137681038CG
rs6927172247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014NA6137681038CG
rs6947392110246325824PRDX5umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.0023670322010LOC1027238781164329761AG
rs69473921102463102723878LOC102723878umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.122010LOC1027238781164329761AG
rs696249714617097TLR2umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.0087297472014NFKBIA1435401887CT
rs696249714617099TLR4umls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1828426212014NFKBIA1435401887CT
rs696249714615468PPARGumls:C0010346BeFreeThe polymorphisms TLR2 (rs1816702), NFKB1 (rs28362491), TNFRSF1A (rs4149570), IL6R (rs4537545), IL23R (rs11209026) and PTPN22 (rs2476601) were associated with risk of CD and the polymorphisms TLR2 (rs1816702), TLR4 (rs1554973 and rs12377632), TLR9 (rs352139), LY96 (rs11465996), NFKBIA (rs696), TNFA (rs1800629), TNFRSF1A (rs4149570), IL10 (rs3024505), IL23R (rs11209026), PTPN22 (rs2476601) and PPARG (rs1801282) were associated with risk of UC.0.1260912732014NFKBIA1435401887CT
rs70761562241238822891ZNF365umls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.1373835492012ZNF365;LOC1053783271062655424AG
rs70761562241238822891ZNF365umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.1373835492012ZNF365;LOC1053783271062655424AG
rs72220942477684454106TLR9umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1308253372014MAP3K141745290287TC
rs7222094247768447124TNFumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.4222949572014MAP3K141745290287TC
rs7222094247768444790NFKB1umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0082628082014MAP3K141745290287TC
rs7222094247768447099TLR4umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1828426212014MAP3K141745290287TC
rs72220942477684423643LY96umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014MAP3K141745290287TC
rs7222094247768449020MAP3K14umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0002714422014MAP3K141745290287TC
rs7222094247768443458IFNGumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.1303346542014MAP3K141745290287TC
rs7222094247768447132TNFRSF1Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.098012312014MAP3K141745290287TC
rs7222094247768444695NDUFA2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0046145122014MAP3K141745290287TC
rs7222094247768447097TLR2umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0087297472014MAP3K141745290287TC
rs7222094247768447128TNFAIP3umls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0031813582014MAP3K141745290287TC
rs7222094247768443605IL17Aumls:C0010346BeFreeNineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05).0.0040716282014MAP3K141745290287TC
rs72824902483710264127NOD2umls:C0010346BeFreeMDDC from rs7282490 GG risk-carriers had reduced ICOSL expression and PRR-initiated signaling and this loss-of-function ICOSLG risk allele associated with an ileal Crohn's disease phenotype, similar to polymorphisms in NOD2.0.562014LOC1053771392144195858GA
rs72981516232665589873FCHSD2umls:C0010346GWASCATA genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.0.122013FCHSD21172959855TG
rs7329174232665581997ELF1umls:C0010346GWASCATA genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.0.122013ELF11340983974AG
rs7362892110246356301SLC7A10umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.0023670322010NA1933266156TC
rs7404952110246322904SBNO2umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1247340642010SBNO2191124836AG
rs74236152110246311262SP140umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1223670322010SP1402230252159CT
rs74236152110246311262SP140umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1223670322010SP1402230252159CT
rs744166185873946774STAT3umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.1461892422008STAT31742362183AG
rs744166252863376774STAT3umls:C0010346BeFreeAssociations between STAT3 rs744166 polymorphisms and susceptibility to ulcerative colitis and Crohn's disease: a meta-analysis.0.1461892422014STAT31742362183AG
rs744166185873946774STAT3umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1461892422008STAT31742362183AG
rs74825699212459928856NR1I2umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0069914752011NR1I23119783118GA
rs74825699212459924790NFKB1umls:C0010346BeFreeGenotypes of nuclear factor (NF)-κB (NFKB1) NFκB -94ins/del (rs28362491); peroxisome proliferator-activated receptor (PPAR)-γ (PPARγ) PPARγ Pro12Ala (rs 1801282) and C1431T (rs 3856806); pregnane X receptor (PXR) (NR1I2) PXR A-24381C (rs1523127), C8055T (2276707), and A7635G (rs 6785049); and liver X receptor (LXR) (NR1H2) LXR T-rs1405655-C and T-rs2695121-C were assessed in a Danish case-control study of 327 Crohn's disease patients, 495 ulcerative colitis (UC) patients, and 779 healthy controls.0.0082628082011NR1I23119783118GA
rs751728238507134295MLNumls:C0010346GWASCATGenome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.0.1205428842014MLN;LOC105375024633796256CT
rs751784717435756149233IL23Rumls:C0010346GWASCATGenome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.0.3705974352007IL23R167215986TG
rs751784718383521149233IL23Rumls:C0010346BeFreeThe data show an association of both IL23R SNPs with overall IBD (statistically stronger, rs7517847; odds ratio [OR] = 0.79, 95% confidence interval [CI]: 0.67-0.94, minor allele frequencies: 0.355 in IBD patients versus 0.410 in controls; P = 0.005), somewhat stronger in Crohn's disease (OR = 0.74, 95% CI: 0.61-0.91) than in ulcerative colitis (OR = 0.84, 95% CI: 0.69-1.03).0.3705974352008IL23R167215986TG
rs753051125159710149233IL23Rumls:C0010346BeFreeWe found that IL23R (L310P) variant conferred a protective effect for crohn's disease (CD) but not ulcerative colitis (UC) patients.0.3705974352014IL23R167219704TC
rs75545112110246355765C1orf106umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1202714422010C1orf1061200908434CA
rs7574865187592726775STAT4umls:C0010346BeFreeThe association of STAT4 polymorphism rs7574865 with RA was validated in patients of Spanish origin (for T versus G, P = 1.2 x 10(-6), odds ratio [OR] 1.59, 95% confidence interval [95% CI] 1.31-1.92), and the association was described for the first time in both clinical forms of inflammatory bowel disease, Crohn's disease and ulcerative colitis (for T versus G, P = 0.006, OR 1.29, 95% CI 1.07-1.55), and in type 1 diabetes mellitus (for T versus G, P = 0.008, OR 1.36, 95% CI 1.07-1.71).0.0058198312008STAT42191099907TG
rs7574865204544506775STAT4umls:C0010346BeFreeEvidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.0.0058198312010STAT42191099907TG
rs7624211858739423308ICOSLGumls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.007643982008LOC1053771392144195678GA
rs762421185873948209C21orf33umls:C0010346GWASCATGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.0.1223670322008LOC1053771392144195678GA
rs762421185873948209C21orf33umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.1223670322008LOC1053771392144195678GA
rs76378018088064112744IL17Fumls:C0010346BeFreeRole of the novel Th17 cytokine IL-17F in inflammatory bowel disease (IBD): upregulated colonic IL-17F expression in active Crohn's disease and analysis of the IL17F p.His161Arg polymorphism in IBD.0.0029099162008IL17F;LOC105375088652236941TC
rs76378018088064149233IL23Rumls:C0010346BeFreeGiven the association of IL23R with inflammatory bowel disease (IBD), we characterized the role of IL-17F in IBD including its intestinal gene expression and the effect of the IL17F p.His161Arg polymorphism on disease susceptibility and phenotype of Crohn's disease (CD) and ulcerative colitis (UC).0.3705974352008IL17F;LOC105375088652236941TC
rs76418789216729393605IL17Aumls:C0010346BeFreeA case-control analysis showed that development of Crohn's disease is associated with the IL-23R variant G149R (OR 0.32, 95% CI 0.15 to 0.68) and IL-17A variant IVS1+18G>C (OR 10.65, 95% CI 1.32 to 85.89).0.0040716282011IL23R167182913GA
rs7641878921672939149233IL23Rumls:C0010346BeFreeA case-control analysis showed that development of Crohn's disease is associated with the IL-23R variant G149R (OR 0.32, 95% CI 0.15 to 0.68) and IL-17A variant IVS1+18G>C (OR 10.65, 95% CI 1.32 to 85.89).0.3705974352011IL23R167182913GA
rs7641878923850713149233IL23Rumls:C0010346GWASCATGenome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.0.3705974352014IL23R167182913GA
rs770233121102463134288TMEM174umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.0023670322010LOC105379031573255307AG
rs770592422412388100861468LINC00492umls:C0010346GWASCATA genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.0.122012LINC00491;LINC004925102611094AG
rs770592422412388133482SLCO6A1umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.0023670322012LINC00491;LINC004925102611094AG
rs7765379232665589966TNFSF15umls:C0010346BeFreeWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.1648303112013NA632713151TG
rs7765379232665586774STAT3umls:C0010346BeFreeWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.1461892422013NA632713151TG
rs7765379232665583133HLA-Eumls:C0010346BeFreeWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.0016286512013NA632713151TG
rs780093211024632646GCKRumls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1271010962010GCKR227519736TC
rs780093211024632646GCKRumls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1271010962010GCKR227519736TC
rs78072681755430026047CNTNAP2umls:C0010346GAD[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]0.0023670322007LOC1053755577148560956GC
rs79278941858739456946C11orf30umls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0047340642008NA1176590272CT
rs8005161211024638477GPR65umls:C0010346GWASCATGenome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.0.1223670322010GPR651488006251CT
rs8005161211024638477GPR65umls:C0010346GAD[Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.]0.1223670322010GPR651488006251CT
rs86474523128233221895JAZF1umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012JAZF1728140937TC
rs88820821514341159296NKX2-3umls:C0010346BeFreeA total of 344 patients with Crohn's disease (CD), 253 patients with ulcerative colitis (UC), and 243 healthy controls (HCs) were genotyped for 3 tag-single nucleotide polymorphisms (SNPs; rs10883365, rs888208, and rs11596008) around NKX2.3.0.2743860362011NKX2-31099536106AG
rs928687918587394356FASLGumls:C0010346GAD[Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.]0.0123780442008NA1172893094AG
rs9292777224123881601DAB2umls:C0010346GAD[A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.]0.0165692242012NA540437846CT
rs9292777175542611601DAB2umls:C0010346GAD[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]0.0165692242007NA540437846CT
rs9469220175543003119HLA-DQB1umls:C0010346GAD[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]0.0050055062007NA632690533GA
rs94916972312823384870RSPO3umls:C0010346GWASCATHost-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.0.122012RSPO3;LOC1053779886127134977AG
rs9858542175543004485MST1umls:C0010346GAD[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]0.2558308432007BSN349664550GA
rs9858542175543008927BSNumls:C0010346GWASCATGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.0.1344736342007BSN349664550GA
rs9858542175542618927BSNumls:C0010346GAD[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]0.1344736342007BSN349664550GA
rs9858542175543008927BSNumls:C0010346GAD[Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.]0.1344736342007BSN349664550GA
rs9858542175542618927BSNumls:C0010346GWASCATSequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.0.1344736342007BSN349664550GA
rs9858542175542614485MST1umls:C0010346GAD[Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.]0.2558308432007BSN349664550GA
rs9891119232665586774STAT3umls:C0010346GWASCATWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.1461892422013STAT31742355962AC
rs9891119232665586774STAT3umls:C0010346BeFreeWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.1461892422013STAT31742355962AC
rs9891119232665589966TNFSF15umls:C0010346BeFreeWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.1648303112013STAT31742355962AC
rs9891119232665583133HLA-Eumls:C0010346BeFreeWe confirmed associations of Crohn's disease with variants in MHC (rs7765379, P = 2.11 × 10(-59)), TNFSF15 (rs6478106, P = 3.87 × 10(-45)), and STAT3 (rs9891119, P = 2.24 × 10(-14)).0.0016286512013STAT31742355962AC
rs998864217804789149233IL23Rumls:C0010346GWASCATGenome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.0.3705974352007IL23R167260421TC
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:1143)
CHR POS SNPID REF ALT ORI_SNPID PMID P_VALUE P_VALUE_TEXT OR/BETA CI95_TEXT GWAS_INITIAL_SAMPLE_SIZE SUB_POPULATION SUPER_POPULATION GWAS_TRAIT HPO_ID HPO_TERM DO_ID DO_TERM MESH_ID MESH_TERM EFO_ID EFO_TERM DOLITE_TERM RISK_ALLELE PUBLICATION_TYPE AA GENE_SYMBOL TYPE REFGENE
16672729rs11583755ACrs11583755236659632.30E-05NA1.67NA983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
17832212rs707458CTrs707458185873946.82E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
17879063rs2797685CTrs2797685211024637.00E-09NA1.05[1.01-1.10] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2797685-AResearch Support, N.I.H., ExtramuralMeta-Analysis
17906008rs707472GTrs707472185873943.63E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
115440156rs6659639GArs6659639176845445.17E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
119718824rs7667GArs7667224828048.00E-06NA1.11NA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
123160272rs4654821TA,C,Grs4654821205709664.40E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
125273200rs7551188TCrs7551188232665589.00E-06NA1.18[1.10-1.28] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7551188-TResearch Support, Non-U.S. Gov'tComparative Study
139164153rs10493084GArs10493084176845441.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
149463801rs3118223GArs3118223176845448.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
164231541rs2819130GArs2819130174357562.10E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
164277035rs596985AGrs596985238507134.13E-05NA1.31[1.15-1.48]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers596985-AResearch Support, Non-U.S. Gov'tValidation Studies
167370292rs1925411CTrs1925411178047894.20E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167372061rs1983860GTrs1983860178047893.58E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167449941rs4620509AGrs4620509178047896.13E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
167460791rs4486425TCrs4486425178047895.47E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167510857rs2815380GArs2815380178047898.04E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
167512695rs1024228AGrs1024228178047891.23E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167513574rs2208577ACrs2208577178047898.91E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
167517022rs2755259TCrs2755259178047891.87E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167521736rs2755262TCrs2755262178047892.01E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167525043rs11208994AGrs11208994178047891.51E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167529243rs2755263AGrs2755263178047895.13E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
167579395rs17129659CTrs17129659178047898.32E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167590461rs11209002TCrs11209002178047892.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167599657rs4655679CTrs4655679178047892.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167601132rs11209003GTrs11209003178047891.00E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167607082rs9729046CGrs9729046178047895.87E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167611613rs4655683GArs4655683170682232.95E-04NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralA
167611613rs4655683GArs4655683178047894.76E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
167615487rs10889657TCrs10889657178047892.31E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167623298rs11209008GArs11209008178047898.79E-09NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167625309rs10889661TArs10889661178047893.56E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167635475rs10889664CTrs10889664178047894.15E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167648596rs76418789GArs76418789238507132.00E-10NA2.06[1.64-2.58]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers76418789-GResearch Support, Non-U.S. Gov'tValidation Studies
167653010rs2064689GArs2064689170682238.52E-05NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralG
167653010rs2064689GArs2064689178047891.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167655147rs17375018GArs17375018178047898.71E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167656931rs12401432CGrs12401432178047896.44E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167662622rs10489630ACrs10489630170682237.07E-05NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralT
167662622rs10489630ACrs10489630178047891.26E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167664154rs714512TGrs714512178047891.60E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167665543rs7556198AGrs7556198178047891.48E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167670133rs1004820TGrs1004820178047894.58E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
167670213rs1004819GArs1004819170682231.78E-14NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralC
167670213rs1004819GArs1004819178047896.25E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167670916rs2902440GArs2902440178047898.81E-09NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167672765rs7539625GArs7539625178047892.15E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167675516rs11805303CTrs11805303175543006.00E-12NA1.39[1.22-1.58]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11805303-TMulticenter StudyResearch Support, N.I.H., Extramural
167675516rs11805303CTrs11805303185873941.82E-39NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
167675728rs10889669TGrs10889669178047896.53E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167679990rs2019262GArs2019262178047899.20E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167681669rs7517847TGrs7517847174357563.00E-12NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
167681669rs7517847TGrs7517847178047897.80E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167685443rs7518660GArs7518660178047896.18E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167685598rs11465802ACrs11465802178047895.04E-07NA2.56[1.75-3.70]382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
167687064rs10789228CTrs10789228178047891.00E-04NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167688349rs10489629TCrs10489629170682231.62E-11NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralG
167694202rs2201841AGrs2201841170682231.10E-14NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralT
167694202rs2201841AGrs2201841178047893.16E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167696547rs12031203GArs12031203178047891.33E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167699254rs11804284TCrs11804284178047892.64E-17NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167701765rs12030948GTrs12030948170682233.33E-05NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralG
167702526rs11465804TGrs11465804170682233.33E-16NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralT
167702526rs11465804TGrs11465804174478423.50E-15NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167702526rs11465804TGrs11465804178047892.08E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167702526rs11465804TGrs11465804185873947.00E-63NA2.5NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11465804-TResearch Support, N.I.H., ExtramuralMeta-Analysis
167702526rs11465804TGrs11465804205709661.00E-06NA1.89[1.47-2.44]896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
167704107rs10489628GArs10489628170682231.96E-04NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralT
167705958rs11209026GArs11209026174478422.00E-18NA2.92NA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167705958rs11209026GArs11209026176845442.17E-07NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167705958rs11209026GArs11209026178047891.32E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167705958rs11209026GArs11209026185873942.15E-68NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
167705958rs11209026GArs11209026211024631.00E-64NA2.66[2.36-3.00]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11209026-GResearch Support, N.I.H., ExtramuralMeta-Analysis
167705958rs11209026GArs11209026222936884.00E-21NA3.18[2.91-3.44]16,179 European ancestry individualsEuropean(16179)ALL(16179)EUR(16179)ALL(16179)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
167705958rs11209026GArs11209026224123881.00E-18NA2.2[2.10-2.35]737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11209026-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
167705958rs11209026GArs11209026229366694.00E-14NA2.84NA1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11209026-GResearch Support, Non-U.S. Gov'tG
167708670rs6682033AGrs6682033170682234.10E-04NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralA
167719129rs1343151GArs1343151170682232.74E-12NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralT
167719129rs1343151GArs1343151174478422.30E-09NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167719129rs1343151GArs1343151178047893.16E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167722567rs10889676CArs10889676178047893.36E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167725120rs10889677CArs10889677170682233.40E-14NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralC
167725120rs10889677CArs10889677174478422.40E-06NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167725120rs10889677CArs10889677178047892.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167726104rs9988642TCrs9988642178047893.16E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167728018rs12567232GArs12567232178047892.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167730055rs6669582AGrs6669582178047891.38E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
167730628rs10789230GTrs10789230178047892.37E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167731368rs7547569TCrs7547569178047892.99E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167732603rs7539328GArs7539328170682238.44E-07NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralG
167735948rs11583760CTrs11583760178047893.95E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167740092rs11209032GArs11209032170682235.50E-13NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralG
167744500rs11209033CGrs11209033178047891.44E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
167747415rs12119179ACrs12119179178047898.36E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
167750474rs7546245TCrs7546245178047894.71E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
167752671rs11209040GA,Crs11209040178047898.43E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
167753508rs1495965CTrs1495965170682233.55E-09NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralG
167760140rs924080TCrs924080170682233.83E-06NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralT
178623626rs17391694CTrs17391694231282333.00E-09NA1.13[1.08-1.19] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers17391694-CResearch Support, N.I.H., ExtramuralMeta-Analysis
182210952rs1391475TCrs1391475205709661.70E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
198928937rs770918AGrs770918176845449.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
199458974rs10489924TCrs10489924176845447.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1111823220rs4323713GTrs4323713176845444.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1114303808rs6679677CArs6679677185873944.95E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1114303808rs6679677CArs6679677231282332.00E-15NA1.2[1.13-1.27] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6679677-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1114377568rs2476601AGrs2476601185873941.00E-08NA1.31NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2476601-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1114377568rs2476601AGrs2476601211024634.00E-09NA1.26[1.17-1.37] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2476601-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1120451190rs3897478TCrs3897478231282332.00E-11NA1.16[1.10-1.22] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3897478-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1147023894rs10494251CTrs10494251176845449.83E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1147108260rs10494248GArs10494248176845447.90E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1147254256rs1342705CTrs1342705176845442.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1147254569rs10494257TCrs10494257176845445.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1155230131rs1142287CTrs1142287211024632.00E-13NANANA6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1155230131rs1142287CTrs3180018211024632.00E-13NA1.13[1.06-1.19]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3180018-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1155282829rs11264359AGrs11264359205709663.80E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1155478897rs6688636TCrs6688636205709664.30E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1160830268rs4656940AGrs4656940211024636.00E-07NA1.15[1.09-1.21] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4656940-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1160852046rs2274910TCrs2274910185873941.00E-09NA1.14NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2274910-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1160878913rs11265519CArs11265519185873943.82E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1162930820rs2343331CTrs2343331174357562.49E-05NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1172853460rs7517810CTrs7517810211024632.00E-15NA1.22[1.16-1.28] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7517810-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1172862234rs9286879AGrs9286879185873942.00E-09NA1.19NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9286879-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1172862234rs9286879AGrs9286879231282336.00E-22NA1.13[1.08-1.17] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9286879-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1172862939rs10489276CTrs10489276185873949.01E-08NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1172898377rs12035082TCrs12035082175542612.00E-07 1.14[1.02-1.27] 1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1190442971rs2490271GArs2490271174357563.44E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1191559356rs10801047ATrs10801047175542613.00E-08 1.47[1.22-1.76] 1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1192559646rs10489873GArs10489873224828047.42E-06NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1197727642rs1998598AGrs1998598211024639.00E-09NA1.04[1.00-1.09] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1998598-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1197743506rs1539414GArs1539414205709664.70E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1200877562rs7554511CArs7554511211024632.00E-07NA1.14[1.08-1.19] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7554511-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1200935866rs11584383TCrs11584383185873941.00E-11NA1.18NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11584383-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1200960307rs2297909GArs2297909185873948.10E-10NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1204789624rs2208843GArs2208843224828045.83E-05NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1206939904rs3024505GArs3024505211024632.00E-14NA1.12[1.07-1.17]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3024505-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1209723420rs6673693TGrs6673693176845446.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1226385623rs10753415TCrs10753415185873945.08E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1228880021rs1062060CTrs1062060205709664.20E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
25664008rs11894081GTrs11894081232665584.00E-09NA1.22[1.20-1.22] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11894081-TResearch Support, Non-U.S. Gov'tComparative Study
221952204rs6733000CTrs6733000174357563.03E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
223932461rs2712102CTrs2712102205709668.40E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
225492467rs13428812AGrs13428812211024639.00E-10NA1.06[1.03-1.10]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers13428812-GResearch Support, N.I.H., ExtramuralMeta-Analysis
227635463rs1728918AGrs1728918231282335.00E-16NA1.12[1.09-1.16] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1728918-AResearch Support, N.I.H., ExtramuralMeta-Analysis
227730940rs1260326TCrs1260326185873942.30E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
227741237rs780094TCrs780094185873941.50E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
227742603rs780093TCrs780093211024635.00E-11NA1.15[1.10-1.21]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers780093-TResearch Support, N.I.H., ExtramuralMeta-Analysis
228582597rs10184619CTrs10184619224828045.85E-06NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
237599337rs7582749CGrs7582749176845443.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
243806918rs10495903CTrs10495903211024632.00E-14NA1.14[1.09-1.20]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10495903-TResearch Support, N.I.H., ExtramuralMeta-Analysis
256448266rs10490395ACrs10490395176845444.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
261186829rs13003464AGrs13003464185873941.57E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
261186829rs13003464AGrs13003464224123885.00E-09NA1.05[1.00-1.40] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers13003464-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
261217542rs10188217TCrs10188217185873946.36E-08NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
261217542rs10188217TCrs10188217212980271.00E-11combinedNANA3,230 European ancestry Crohn's disease cases; 768 European ancestry celiac disease cases; 6,251 European ancestry controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
261224259rs10181042CTrs10181042211024637.00E-09NA1.14[1.09-1.19] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10181042-TResearch Support, N.I.H., ExtramuralMeta-Analysis
262551472rs10865331AGrs10865331231282331.00E-09NA1.1[1.06-1.13] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10865331-AResearch Support, N.I.H., ExtramuralMeta-Analysis
262713533rs6545946CTrs6545946224123887.00E-09NA1.16[1.06-1.27] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6545946-CResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
265702803rs840969TCrs840969238507138.59E-05NA1.18[1.09-1.28]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers840969-TResearch Support, Non-U.S. Gov'tValidation Studies
266082204rs2194782AGrs2194782205709661.60E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2102622376rs4851527AGrs4851527224828042.26E-05NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
2102971865rs13015714GTrs13015714212980271.63E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2103019919rs1035127AGrs1035127212980271.23E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2103024813rs4851007TGrs4851007212980272.11E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2103035044rs1420106AGrs1420106212980272.53E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2103038587rs3755267TGrs3755267212980271.49E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2103049910rs2041756AGrs2041756212980273.25E-05NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2103054449rs2058660GArs2058660211024632.00E-12NA1.19[1.14-1.26]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2058660-GResearch Support, N.I.H., ExtramuralMeta-Analysis
2103063369rs6708413GArs6708413185873941.45E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2103063369rs6708413GArs6708413212980272.05E-05NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2103068787rs7559479GArs7559479212980273.03E-05NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2103070568rs917997TCrs917997185873941.11E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2103070568rs917997TCrs917997212980272.17E-05NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2103094213rs759382GTrs759382212980272.03E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2123186585rs10496586CTrs10496586176845443.90E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
2125426455rs4848966TGrs4848966232665587.55E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
2145504693rs7603516TGrs7603516174357563.10E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
2160964700rs10497212TGrs10497212176845447.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
2161101169rs2925757GArs2925757176845442.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
2165985503rs17829596TCrs17829596205709665.70E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2180216731rs13403289CArs13403289236659634.10E-05NA1.67NA983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2180216731rs13403289CArs13403289236659634.60E-05NA1.67NA239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2181339431rs934882GArs934882205709664.30E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2198113157rs2697290AGrs2697290205709669.80E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2198896895rs6738825AGrs6738825211024634.00E-09NA1.06[1.02-1.11] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6738825-AResearch Support, N.I.H., ExtramuralMeta-Analysis
2223930506rs9283536CTrs9283536176845447.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
2231091223rs13397985TGrs13397985185873949.04E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2231097129rs6716753TCrs6716753231282331.00E-16NA1.13[1.09-1.18] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6716753-CResearch Support, N.I.H., ExtramuralMeta-Analysis
2231109329rs6743984TCrs6743984185873942.48E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2231116874rs7423615CTrs7423615211024633.00E-13NA1.12[1.07-1.18]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7423615-TResearch Support, N.I.H., ExtramuralMeta-Analysis
2234158839rs10210302CTrs10210302175543005.00E-14NA1.19[1.01-1.41]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10210302-TMulticenter StudyResearch Support, N.I.H., Extramural
2234173503rs12994997GArs12994997231282334.00E-70NA1.23[1.19-1.27] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers12994997-AResearch Support, N.I.H., ExtramuralMeta-Analysis
2234180410rs3828309AGrs3828309185873942.00E-32NA1.25NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3828309-GResearch Support, N.I.H., ExtramuralMeta-Analysis
2234183368rs2241880AGrs2241880174357561.00E-13NA1.45[1.27-1.64]946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2241880-GResearch Support, N.I.H., ExtramuralComparative Study
2234183368rs2241880AGrs2241880176845448.68E-07NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
2234183368rs2241880AGrs2241880185873944.61E-25NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2234183368rs2241880AGrs2241880205709663.00E-06NA1.32[1.18-1.47]896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2234183368rs2241880AGrs2241880224123881.00E-12NA1.32[1.24-1.41]737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2241880-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2234184417rs3792109GArs3792109211024637.00E-41NA1.34[1.29-1.40]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3792109-AResearch Support, N.I.H., ExtramuralMeta-Analysis
2234184417rs3792109GArs3792109229366695.00E-09NA1.38NA1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3792109-AResearch Support, Non-U.S. Gov'tT
2234210681rs4663147GArs4663147238507136.05E-05NA1.31[1.15-1.49]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4663147-GResearch Support, Non-U.S. Gov'tValidation Studies
2235446253rs7592582ACrs7592582205709661.00E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
318706858rs13073817GArs13073817211024637.00E-09NA1.08[1.03-1.13] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers13073817-AResearch Support, N.I.H., ExtramuralMeta-Analysis
335539957rs940070CGrs940070176845444.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
337574024rs267567GArs267567185873943.03E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
349326178rs9874474AGrs9874474178047891.31E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349329090rs4410472ATrs4410472178047891.53E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349343175rs2230929GA,C,Trs2230929178047891.38E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349359943rs9873994TCrs9873994178047891.63E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349366741rs9863142GCrs9863142178047891.32E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349389842rs17080528CTrs17080528178047898.75E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349406080rs2878298TCrs2878298178047894.62E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tNA
349411404rs7621003TCrs7621003178047894.76E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349416825rs7648841GArs7648841178047893.63E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349450864rs6784820AGrs6784820185873941.20E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
349453834rs6997CTrs6997178047893.16E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349459114rs4855873ACrs4855873178047893.25E-15NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349463287rs6446272GArs6446272178047894.17E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349470668rs7646366GArs7646366178047895.82E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349497883rs885592TGrs885592178047891.61E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
349499829rs10865955GArs10865955178047892.81E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349520958rs1568661AGrs1568661178047891.92E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
349521974rs4855864CTrs4855864178047892.03E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349524236rs3924462TGrs3924462185873943.56E-08NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
349525962rs4855861GTrs4855861178047891.53E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349535115rs7637999CTrs7637999178047891.41E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349538799rs11130199TCrs11130199178047891.85E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349557051rs3870338AGrs3870338178047891.45E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349570882rs1050088TCrs1050088178047891.40E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349580347rs11720264CTrs11720264178047891.79E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349590770rs3811697CTrs3811697178047893.19E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349626306rs6446285GArs6446285178047891.97E-04NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
349634696rs9875617GArs9875617178047891.95E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349649989rs9827708CGrs9827708178047896.61E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349666964rs1873625CArs1873625178047896.61E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349675142rs1873626TArs1873626178047891.92E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349679072rs2329021GArs2329021178047892.69E-09NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349682311rs9812791GArs9812791178047891.61E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG,A
349696797rs11718165AGrs11718165178047891.48E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
349701983rs9858542GArs9858542175542615.00E-08 1.17[1.14-1.31] 1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349701983rs9858542GArs9858542175543004.00E-08NA1.09[0.96-1.24]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9858542-AMulticenter StudyResearch Support, N.I.H., Extramural
349701983rs9858542GArs9858542185873943.55E-12NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
349714225rs1131095TCrs1131095178047891.99E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349715446rs4855881GArs4855881178047891.09E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349719729rs9822268GArs9822268178047891.26E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349721532rs3197999GArs3197999185873941.00E-12NA1.2NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3197999-AResearch Support, N.I.H., ExtramuralMeta-Analysis
349721532rs3197999GArs3197999211024636.00E-17NA1.22[1.16-1.27]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3197999-AResearch Support, N.I.H., ExtramuralMeta-Analysis
349772375rs7649348GArs7649348178047892.09E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
349788969rs7372966TCrs7372966178047892.36E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349790544rs7372725CArs7372725178047891.52E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349807085rs9859153GTrs9859153178047892.62E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349819102rs11130221CGrs11130221178047892.33E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349842625rs2234391AGrs2234391178047891.35E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC,T
349869158rs695238ACrs695238178047891.09E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349882349rs2247036CTrs2247036178047891.16E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349890613rs2352974CTrs2352974178047892.02E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
349898000rs2777888AGrs2777888178047891.32E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
349902544rs9821675AGrs9821675178047892.57E-04NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG,A
349924424rs11713193GArs11713193178047892.57E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
349936102rs2230590TCrs2230590178047893.91E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
349949834rs7634084ATrs7634084178047893.20E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
350210289rs1005678CGrs1005678178047899.95E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
350212512rs2624833GTrs2624833178047895.45E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
359736299rs812965TCrs812965176845444.80E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
3106624294rs1517605TCrs1517605212980271.98E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
3106639719rs1568206CGrs1568206212980272.90E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
3113272208rs1513287GArs1513287176845449.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
3113680951rs1386478AGrs1386478224828047.00E-06NA1.12NA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
3121551570rs12695416AGrs12695416178047896.31E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
3132192129rs9829140TCrs9829140185873946.21E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
3133575865rs7644124TCrs7644124176845442.90E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
3138992418rs10513059CTrs10513059176845442.07E-06NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
3140169657rs6439924ACrs6439924174357566.00E-05NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
3175151789rs10490876CTrs10490876176845443.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
3192595307rs2367129ACrs2367129176845441.90E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
46206784rs10003892GArs10003892178047893.65E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
46213622rs4274923GArs4274923178047893.00E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
46216955rs13132796CGrs13132796178047895.83E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
46219929rs4234723AGrs4234723178047894.89E-04NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
46222105rs908016ATrs908016178047892.81E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
47531319rs11931489GArs11931489185873945.27E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
437967083rs10517460ACrs10517460176845441.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
438322491rs76273539GTrs76273539232665588.35E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438324906rs4453942ACrs4453942232665584.68E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438325003rs1906295GArs1906295232665584.81E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438325036rs6856616TCrs6856616232665583.57E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438325036rs6856616TCrs6856616238507134.00E-14NA1.43[1.31-1.57]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6856616-CResearch Support, Non-U.S. Gov'tValidation Studies
438325062rs1906296GArs1906296232665586.52E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438325105rs1906297TCrs1906297232665585.80E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438327654rs6822641AGrs6822641232665585.85E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438328777rs6829875AGrs6829875232665585.94E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438330016rs73243350GArs73243350232665581.15E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438335067rs73243351GArs73243351232665581.51E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438335823rs1487630CTrs1487630232665581.00E-11NA1.33[1.22-1.44] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1487630-TResearch Support, Non-U.S. Gov'tComparative Study
438337114rs75918970CTrs75918970232665581.84E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438345898rs73243354ACrs73243354232665581.16E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438361416rs55843528GArs55843528232665581.72E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438363406rs6846728TGrs6846728232665581.51E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438364637rs62294142GArs62294142232665583.19E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438367910rs55818238TCrs55818238232665581.12E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438369359rs73243363CTrs73243363232665582.14E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
438379303rs12330996CTrs12330996232665581.88E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
441753130rs16853571ACrs16853571174357562.40E-07NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
448363983rs6837335AGrs6837335231282332.00E-08NA1.09[1.05-1.12] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6837335-GResearch Support, N.I.H., ExtramuralMeta-Analysis
476134763rs1845983GArs1845983176845444.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
476161222rs7681167AGrs7681167176845442.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
4102865304rs13126505GArs13126505231282332.00E-12NA1.17[1.10-1.25] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers13126505-AResearch Support, N.I.H., ExtramuralMeta-Analysis
4104665738rs233991CArs233991205709665.40E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
4106106353rs10010325CArs10010325185873945.03E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
4110175673rs115921721AGrs115921721232665587.48E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
4134471862rs1493517CTrs1493517176845445.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
4134487011rs9307696GCrs9307696176845445.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
4134530386rs925084TGrs925084176845441.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
4134536988rs7674505GArs7674505176845442.63E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
4134554855rs2660727GArs2660727176845443.95E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
4134600991rs7700170GArs7700170176845442.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
4134619611rs2660693CGrs2660693176845442.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
4138225217rs1559781CTrs1559781176845444.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
4149835012rs853727CTrs853727176845442.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
4157145352rs10517634CTrs10517634176845445.50E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
4187201211rs5974AGrs5974185873947.81E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
4187210620rs4253431GArs4253431185873941.33E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
516178920rs342549GArs342549232665584.84E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
525781613rs2928266TCrs2928266176845442.80E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
537913544rs10512670ACrs10512670185873942.41E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
540319877rs1445002CArs1445002176845443.94E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
540320006rs348601TCrs348601174478425.10E-07NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
540372223rs7725523AGrs7725523176845447.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
540386555rs1002922TCrs1002922174478421.70E-09NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
540392728rs4613763TCrs4613763174357561.21E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
540392728rs4613763TCrs4613763174478421.20E-09NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
540392728rs4613763TCrs4613763185873947.00E-27NA1.32NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4613763-CResearch Support, N.I.H., ExtramuralMeta-Analysis
540393605rs10512734AGrs10512734174478429.20E-11NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
540393852rs1992662AGrs1992662176845441.56E-07NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
540401509rs17234657TGrs17234657175543002.00E-12NA1.54[1.34-1.76]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers17234657-GMulticenter StudyResearch Support, N.I.H., Extramural
540401509rs17234657TGrs17234657185873943.41E-27NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
540410584rs11742570TCrs11742570211024637.00E-36NA1.33[1.27-1.39]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11742570-CResearch Support, N.I.H., ExtramuralMeta-Analysis
540410584rs11742570TCrs11742570229366691.00E-06NA1.32NA1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11742570-CResearch Support, Non-U.S. Gov'tC
540415067rs1992660CTrs1992660176845444.00E-07NA1.42[1.24-1.67]393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
540431183rs1373692ACrs1373692174357565.37E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
540431183rs1373692ACrs1373692174478422.00E-12NA1.46NA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
540437948rs9292777CTrs9292777175542613.00E-18NA1.34[1.20-1.50]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
540437948rs9292777CTrs9292777224123882.00E-11NA1.37[1.28-1.48]737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9292777-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
540463739rs4957300TCrs4957300176845442.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
540477515rs4495224CArs4495224174478422.20E-07NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
540487270rs7725052CTrs7725052176845443.24E-06NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
540502932rs1553575AGrs1553575176845441.68E-06NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
540554269rs6451525CTrs6451525176845441.64E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
545266589rs4866929AGrs4866929205709669.10E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
555438851rs10065637CTrs10065637231282334.00E-12NA1.12[1.08-1.17] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10065637-CResearch Support, N.I.H., ExtramuralMeta-Analysis
572551134rs7702331AGrs7702331211024636.00E-12NA1.12[1.07-1.17]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7702331-AResearch Support, N.I.H., ExtramuralMeta-Analysis
572551134rs7702331AGrs7702331231282336.00E-10NA1.09[1.05-1.13] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7702331-AResearch Support, N.I.H., ExtramuralMeta-Analysis
584758140rs247660ACrs247660185873947.30E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
594649904rs255969CTrs255969178047891.41E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
596244549rs2549794CTrs2549794211024631.00E-10NA1.05[1.02-1.09]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2549794-CResearch Support, N.I.H., ExtramuralMeta-Analysis
5101946798rs7705924AGrs7705924224123882.00E-08NA1.48[1.17-1.87] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7705924-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
5115022257rs249721AGrs249721176845442.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5115891083rs254079AGrs254079185873942.55E-17NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
5129149447rs10053519AGrs10053519224828044.42E-06NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
5129436666rs10050470GArs10050470178047895.07E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5129439574rs6858978AGrs6858978178047897.14E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5129669537rs6595948CTrs6595948178047894.93E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5129684556rs6869287GTrs6869287178047898.81E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130104076rs10051722ACrs10051722178047895.38E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5130603119rs6596008AGrs6596008178047893.87E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130611700rs1468328ATrs1468328178047895.56E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130616792rs12513768GArs12513768178047892.96E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5130626621rs11242070AGrs11242070178047892.34E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130657418rs2549011GCrs2549011178047892.31E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tNA
5130657418rs35707316GGCrs2549011178047892.31E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tNA
5130674076rs4706020GArs4706020178047893.61E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5130688378rs798407CGrs798407178047892.85E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5130709422rs30735GArs30735178047891.94E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130740005rs257391CArs257391178047891.15E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130753077rs10040442CGrs10040442178047895.83E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5130769785rs6596024CArs6596024178047893.03E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130773561rs6896132GCrs6896132178047891.78E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5130802970rs3776027TCrs3776027178047892.89E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130808198rs31241TCrs31241178047892.10E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130811146rs31240TArs31240178047894.25E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130813377rs31239TGrs31239178047892.09E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130824536rs31258GArs31258178047893.70E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130828649rs39600ATrs39600178047893.70E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130831365rs40400TCrs40400178047894.25E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130833433rs31252TCrs31252178047892.19E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130837077rs7720194TCrs7720194178047892.37E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130855000rs4705890TCrs4705890178047892.32E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130867404rs3776013CTrs3776013178047892.42E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5130872520rs994453TGrs994453178047892.05E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130875538rs3776006CTrs3776006178047892.10E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5130891101rs984616CTrs984616178047897.10E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5130902196rs9327616CTrs9327616178047892.77E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5130907189rs8180462TCrs8180462178047892.67E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130911578rs11750704CArs11750704178047894.25E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5130918037rs9687376ACrs9687376178047892.77E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130920831rs2021774GArs2021774178047895.36E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5130926822rs3756291TCrs3756291178047896.15E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130935777rs11242084TCrs11242084178047892.71E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130942624rs1422870GTrs1422870178047891.13E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5130951750rs3756290AGrs3756290178047898.13E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130957992rs3776001TArs3776001178047892.13E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5130966026rs6872682TCrs6872682178047893.13E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130982194rs3756289AGrs3756289178047892.64E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5130990384rs26003TCrs26003178047892.64E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131006082rs27450AGrs27450178047892.38E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131013815rs26010GArs26010178047892.73E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131048122rs32112GArs32112178047891.82E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131055546rs548635TGrs548635178047892.68E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5131072410rs10051003CTrs10051003178047892.10E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5131099227rs1019122CTrs1019122178047892.22E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5131107381rs3775992TGrs3775992178047891.92E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131114979rs10042334ATrs10042334178047892.07E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131118943rs9327621TCrs9327621178047892.04E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC,T
5131135478rs3756287AGrs3756287178047892.37E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5131146993rs4705901TCrs4705901178047898.41E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5131152575rs11242095TCrs11242095178047892.07E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5131165216rs2133706TGrs2133706178047892.07E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5131174215rs10069521AGrs10069521178047891.86E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131202457rs1875176GArs1875176178047892.07E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131258378rs113905823AACrs630044178047898.55E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5131258378rs630044ACrs630044178047898.55E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5131267609rs578637GArs578637178047892.03E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131269453rs519240GArs519240178047892.10E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131275509rs667437GArs667437178047892.07E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131286708rs648304TCrs648304178047898.09E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5131305384rs40819GTrs40819178047891.84E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131318788rs399714CTrs399714178047892.44E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5131343017rs10040809ACrs10040809178047896.41E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131348878rs246998AGrs246998178047898.63E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131350903rs555662GArs555662178047899.64E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
5131363979rs17132324AGrs17132324178047892.91E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131369168rs3916442GArs3916442178047892.10E-09NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131371999rs1858074AGrs1858074178047898.97E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131379656rs7728344CTrs7728344178047893.29E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5131397202rs31481GArs31481178047894.13E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131401334rs246844GArs246844178047891.41E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131402738rs3091338CTrs3091338224123884.00E-08NA1.23[1.08-1.42] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3091338-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
5131405027rs31474TCrs31474178047892.91E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5131420249rs3864277GArs3864277178047891.17E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131575338rs12521097GArs12521097178047891.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131577894rs2136187TCrs2136187178047891.88E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131582356rs3844312CTrs3844312178047891.10E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131586480rs3763112AGrs3763112178047891.79E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131665423rs272888TCrs272888178047894.79E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5131676320rs1050152CTrs1050152178047892.14E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5131676320rs1050152CTrs1050152185873941.54E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
5131742228rs6596075GCrs6596075175543003.00E-06NA1.55[1.00-2.39]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6596075-CMulticenter StudyResearch Support, N.I.H., Extramural
5131770805rs2188962CTrs2188962185873942.00E-18NA1.25NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2188962-TResearch Support, N.I.H., ExtramuralMeta-Analysis
5131770805rs2188962CTrs2188962205709661.00E-07NA1.36[1.21-1.52]896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
5131784393rs12521868GTrs12521868211024631.00E-20NA1.23[1.18-1.28]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers12521868-TResearch Support, N.I.H., ExtramuralMeta-Analysis
5131801947rs2522057GCrs2522057178047893.16E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5131804347rs2248116CArs2248116178047893.16E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5131833599rs736801CTrs736801178047891.69E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5136447574rs1859346ACrs1859346176845447.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5141479065rs11167764ACrs11167764211024632.00E-09NA1.06[1.02-1.11] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11167764-CResearch Support, N.I.H., ExtramuralMeta-Analysis
5146046418rs3096085GArs3096085176845448.50E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
5150223387rs13361189TCrs13361189175542612.00E-10NA1.38[1.15-1.66]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
5150223387rs13361189TCrs13361189185873947.33E-16NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
5150240076rs1000113CTrs1000113175543003.00E-07NA1.54[1.31-1.82]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1000113-TMulticenter StudyResearch Support, N.I.H., Extramural
5150258867rs11747270AGrs11747270185873943.00E-16NA1.33NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11747270-GResearch Support, N.I.H., ExtramuralMeta-Analysis
5150270420rs7714584AGrs7714584211024638.00E-19NA1.37[1.28-1.47]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7714584-GResearch Support, N.I.H., ExtramuralMeta-Analysis
5158787385rs6556412GArs6556412211024635.00E-14NA1.18[1.13-1.24] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6556412-AResearch Support, N.I.H., ExtramuralMeta-Analysis
5158814533rs10045431ACrs10045431185873944.00E-13NA1.11NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10045431-CResearch Support, N.I.H., ExtramuralMeta-Analysis
5158814533rs10045431ACrs10045431205709667.00E-08NA1.45[1.27-1.64]896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
5158822645rs6887695GCrs6887695175542619.00E-06 1.26[1.12-1.41] 1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
5173279842rs359457CTrs359457211024633.00E-12NA1.08[1.04-1.12]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers359457-TResearch Support, N.I.H., ExtramuralMeta-Analysis
5173337853rs17695092TGrs17695092231282335.00E-09NA1.1[1.05-1.14] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers17695092-TResearch Support, N.I.H., ExtramuralMeta-Analysis
5177802373rs12519834GArs12519834205709665.00E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
6880234rs7768444CArs7768444205709665.60E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
63433318rs17309827TGrs17309827185873943.70E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
63433318rs17309827TGrs17309827211024637.00E-09NA1.1[1.05-1.16] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers17309827-TResearch Support, N.I.H., ExtramuralMeta-Analysis
63434242rs4959830GArs4959830185873942.83E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
65151247rs12529198AGrs12529198185873943.48E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
620689945rs7748720GArs7748720185873941.64E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
620728731rs6908425TCrs6908425185873949.00E-10NA1.21NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6908425-CResearch Support, N.I.H., ExtramuralMeta-Analysis
620728731rs6908425TCrs6908425211024631.00E-08NA1.17[1.11-1.23] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6908425-CResearch Support, N.I.H., ExtramuralMeta-Analysis
621430728rs12663356TCrs12663356231282334.00E-12NA1.1[1.06-1.13] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers12663356-CResearch Support, N.I.H., ExtramuralMeta-Analysis
621457950rs11758386CTrs11758386185873943.40E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
621470419rs7759649CTrs7759649185873945.02E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
628791202rs10484543ATrs10484543176845449.36E-06NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
628968930rs9257453AGrs9257453176845443.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
629234510rs10484545CGrs10484545176845442.84E-07NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
629723161rs9258260CTrs9258260224123882.00E-10NA1.45[1.21-1.68]737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9258260-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
630955681rs1634731GArs1634731232665582.45E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631085770rs3094212GArs3094212232665581.16E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631085770rs551894425GArs3094212232665581.16E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631111356rs9263739CTrs9263739232665587.11E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631114573rs2240064GArs2240064232665585.23E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631119589rs1265109GTrs1265109232665582.05E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631125569rs2239524TGrs2239524232665583.03E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631126944rs3094187CTrs3094187232665581.37E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631130593rs1419881GArs1419881232665582.36E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631133943rs3130932CArs3130932232665589.90E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631134888rs3130931TCrs3130931232665583.43E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631136453rs3130501AGrs3130501232665582.22E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631142245rs3094188CArs3094188232665587.00E-07NA1.61[1.33-1.94] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3094188-CResearch Support, Non-U.S. Gov'tComparative Study
631187075rs3130467CTrs3130467232665587.90E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631209510rs3130712CTrs3130712232665587.24E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631241127rs13207315TCrs13207315232665586.72E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631243884rs3130696GArs3130696232665581.65E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631245736rs6906846AGrs6906846232665582.52E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631263751rs2894207TCrs2894207236659632.90E-05NA1.6[1.30-2.10]983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers2894207-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
631271157rs7750269AGrs7750269232665585.52E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631272157rs9368675GArs9368675232665585.47E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631274380rs9264942TCrs9264942231282335.00E-28NA1.15[1.11-1.18] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9264942-CResearch Support, N.I.H., ExtramuralMeta-Analysis
631275174rs396243TCrs396243232665585.63E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631308630rs9265797GArs9265797232665585.06E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631348580rs9266689AGrs9266689232665585.54E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631349922rs9266722CTrs9266722232665589.80E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631436789rs2523674AGrs2523674232665583.04E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631489644rs3132454AGrs3132454232665581.09E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631542308rs1799964TCrs1799964211024634.00E-11NA1.19[1.13-1.25] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1799964-CResearch Support, N.I.H., ExtramuralMeta-Analysis
631566204rs2509217CTrs2509217232665585.70E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
631575276rs9348876CTrs9348876229366693.00E-06NA1.41[1.22-1.63] 1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9348876-TResearch Support, Non-U.S. Gov'tT
631917540rs4151657TCrs4151657232665583.88E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632050067rs185819TCrs185819232665582.08E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632071893rs3134954CTrs3134954232665585.42E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632144530rs2071290CTrs2071290232665588.61E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632147696rs3130349GArs3130349232665588.58E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632149816rs3134940TCrs3134940232665581.45E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632160153rs2269420CA,G,Trs2269420232665588.45E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632186872rs2256594AGrs2256594232665586.10E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632188823rs8192585GArs8192585232665586.12E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632191339rs3830041CTrs3830041232665584.26E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632192560rs2267644GArs2267644232665582.56E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632199144rs377763CArs377763232665589.18E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632205045rs549182GArs549182232665586.43E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632205110rs9267911TCrs9267911232665583.00E-07NA1.5[1.29-1.76] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9267911-TResearch Support, Non-U.S. Gov'tComparative Study
632209027rs382259TCrs382259232665581.83E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632315727rs910049TCrs910049232665585.44E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632321597rs1265761AGrs1265761232665586.12E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632336766rs3129939AGrs3129939232665581.29E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632373232rs10947261GTrs10947261238507133.00E-12NA1.36[1.25-1.49]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10947261-TResearch Support, Non-U.S. Gov'tValidation Studies
632376471rs3763313ACrs3763313185873942.60E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
632409530rs3129882GArs3129882232665584.79E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632411523rs2239804TCrs2239804232665588.86E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632569691rs477515GArs477515232665582.28E-07NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632570400rs2516049TCrs2516049232665582.33E-07NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632577380rs660895AGrs660895232665582.04E-10NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632578052rs532098GArs532098232665585.43E-08NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632586854rs9271366GArs9271366232665582.80E-09NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632586854rs9271366GArs9271366238507135.00E-12NA1.66[1.44-1.92]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9271366-AResearch Support, Non-U.S. Gov'tValidation Studies
632627714rs1063355TGrs1063355232665582.65E-07NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632652317rs7755224AG,Trs7755224232665589.93E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632658310rs9469220GArs9469220175543002.00E-06NA1.14[0.98-1.32]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9469220-AMulticenter StudyResearch Support, N.I.H., Extramural
632659878rs9275224AGrs9275224232665582.48E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632663564rs5000634AGrs5000634232665586.99E-08NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632663851rs6457617CTrs6457617232665587.41E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632665728rs9275312AGrs9275312232665587.20E-09NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632666822rs9275328CTrs9275328232665588.28E-09NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632668296rs9275371TCrs9275371232665581.10E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632668526rs9275374CTrs9275374232665589.55E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632669156rs9275390TCrs9275390232665588.88E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632669439rs9275393GArs9275393232665588.69E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632669767rs2647050TCrs2647050232665585.95E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632669955rs9275406GTrs9275406232665588.69E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670000rs2858308GTrs2858308232665587.14E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670037rs9275407GTrs9275407232665588.69E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670110rs9275408TCrs9275408232665588.14E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670244rs9275418AGrs9275418232665588.44E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670255rs2856718CTrs2856718232665586.26E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670576rs9275424AGrs9275424232665588.69E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670874rs9275425CArs9275425232665588.60E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670915rs9275427CTrs9275427232665588.41E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670956rs2856705CTrs2856705232665587.03E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632670978rs9275428AGrs9275428232665588.60E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632671103rs13192471TCrs13192471232665585.67E-08NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632671521rs9275439TCrs9275439232665588.69E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632677912rs9275563CTrs9275563232665581.63E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632678999rs9275572AGrs9275572232665581.38E-09NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632679690rs3129727CTrs3129727232665584.71E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632680928rs7765379TGrs7765379232665589.00E-59NA1.93[1.78-2.09] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7765379-GResearch Support, Non-U.S. Gov'tComparative Study
632680970rs7745656GTrs7745656232665581.53E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632681161rs2858332GTrs2858332232665581.57E-10NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632681277rs2858331AGrs2858331185873942.17E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
632681277rs2858331AGrs2858331232665582.02E-07NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632685685rs3104398GArs3104398232665583.19E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632685865rs9275653GArs9275653232665584.33E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632699515rs2859099CTrs2859099232665582.94E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632702449rs2859078AGrs2859078232665586.49E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632711178rs17500468AGrs17500468232665585.94E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632722186rs10807113CArs10807113232665588.65E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632723917rs7756516CTrs7756516232665588.77E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632741742rs2857210AGrs2857210232665587.01E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632784676rs2071554CTrs2071554232665583.20E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632788511rs9784758TCrs9784758232665583.01E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632797684rs241437AGrs241437232665582.06E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632818678rs2071538GArs2071538232665583.91E-09NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632941910rs620202GTrs620202232665583.88E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632944746rs11908GArs11908232665582.32E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632950050rs565876GArs565876232665582.79E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632955976rs188245AGrs188245232665582.84E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
632962420rs206767CArs206767232665586.40E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633058952rs10484569GArs10484569232665582.38E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633060118rs2281388GArs2281388232665583.25E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633077776rs6457713CTrs6457713232665582.38E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633079166rs9380343CTrs9380343232665585.94E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633086448rs1883414GArs1883414232665586.11E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633097614rs3129269CArs3129269232665582.48E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633098966rs2294478CArs2294478232665581.12E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633099210rs2294472AGrs2294472232665582.09E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633114171rs1003979TCrs1003979232665581.09E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633138021rs9368758GArs9368758232665584.82E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633141253rs9277932TGrs9277932232665582.29E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633141280rs2855430GArs2855430232665583.76E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633142539rs3762013GArs3762013232665582.38E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633154656rs2855459GArs2855459232665583.47E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633158898rs2269346CTrs2269346232665584.82E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633202640rs213220CTrs213220232665581.32E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633252115rs455567GArs455567232665589.02E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
633764033rs751728CTrs751728238507131.00E-08NA1.32[1.20-1.45]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers751728-TResearch Support, Non-U.S. Gov'tValidation Studies
634961360rs3800440GArs3800440232665581.70E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
635162141rs11755266CTrs11755266232665588.47E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
635206553rs732594CArs732594232665587.65E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
635805133rs17704843GArs17704843232665584.95E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
657217336rs12209200CTrs12209200205709661.80E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
670912835rs10498871CTrs10498871176845445.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
681473184rs13201732CGrs13201732178047898.32E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
688776981rs806438TArs806438185873941.00E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
690973159rs1847472CArs1847472211024635.00E-09NA1.07[1.03-1.11] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1847472-GResearch Support, N.I.H., ExtramuralMeta-Analysis
691082136rs4707614GArs4707614176845447.80E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
692576591rs1546210CArs1546210176845444.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
6106435025rs6568421AGrs6568421211024634.00E-08NA1.13[1.07-1.18] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6568421-GResearch Support, N.I.H., ExtramuralMeta-Analysis
6106435269rs7746082GCrs7746082185873942.00E-10NA1.17NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7746082-CResearch Support, N.I.H., ExtramuralMeta-Analysis
6118124150rs495662GArs495662185873943.05E-16NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
6127456122rs9491697AGrs9491697231282334.00E-10NA1.08[1.04-1.11] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9491697-GResearch Support, N.I.H., ExtramuralMeta-Analysis
6128245765rs13204742GTrs13204742231282338.00E-15NA1.17[1.12-1.23] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers13204742-TResearch Support, N.I.H., ExtramuralMeta-Analysis
6149577079rs7758080AGrs7758080185873944.39E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
6159465977rs1738074TCrs1738074212980271.53E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
6159490436rs212388CTrs212388211024632.00E-11NA1.1[1.05-1.14]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers212388-GResearch Support, N.I.H., ExtramuralMeta-Analysis
6159490436rs212388CTrs212388212980272.00E-10combinedNANA3,230 European ancestry Crohn's disease cases; 768 European ancestry celiac disease cases; 6,251 European ancestry controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
6159490436rs212388CTrs212388231282333.00E-14NA1.11[1.07-1.14] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers212388-CResearch Support, N.I.H., ExtramuralMeta-Analysis
6164020325rs9346964GArs9346964236659631.80E-05NA1.7[1.30-2.10]983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers9346964-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
6167371110rs2149085TCrs2149085238507138.00E-12NA1.34[1.23-1.45]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2149085-TResearch Support, Non-U.S. Gov'tValidation Studies
6167383972rs429083TCrs429083232665581.11E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
6167398071rs394522ACrs394522238507139.83E-11NA1.32[1.21-1.43]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers394522-CResearch Support, Non-U.S. Gov'tValidation Studies
6167406633rs415890GCrs415890211024633.00E-12NA1.17[1.12-1.22] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers415890-CResearch Support, N.I.H., ExtramuralMeta-Analysis
6167411008rs400837TCrs400837232665581.83E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
6167435325rs7749278TCrs7749278185873945.80E-10NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
6167437988rs2301436CTrs2301436185873941.00E-12NA1.21NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2301436-TResearch Support, N.I.H., ExtramuralMeta-Analysis
6167437988rs2301436CTrs2301436205709666.00E-08NA1.37[1.22-1.53]896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
6167461562rs10484530CTrs10484530232665588.35E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
6169912559rs2997887AGrs2997887205709663.80E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
73232378rs10272892TCrs10272892236659633.50E-05NA1.67NA239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
74912398rs4720435GTrs4720435205709662.80E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
710372184rs891854TCrs891854205709661.60E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
715041529rs10255000TCrs10255000176845448.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
717405718rs7780687AGrs7780687236659632.70E-05NA2[1.40-2.80]239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers7780687-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
721800459rs6461599AGrs6461599176845447.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
722202485rs1981601TCrs1981601205709665.80E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
724951382rs134GArs134178047892.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
726597211rs6957717AGrs6957717236659634.91E-05NA1.67NA983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
726892440rs10486483GArs10486483231282333.00E-08NA1.09[1.05-1.13] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10486483-AResearch Support, N.I.H., ExtramuralMeta-Analysis
728180556rs864745TCrs864745231282334.00E-09NA1.09[1.05-1.12] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers864745-TResearch Support, N.I.H., ExtramuralMeta-Analysis
731786849rs7795363TCrs7795363176845446.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
734775544rs1419790GTrs1419790176845447.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
741872709rs10486725CTrs10486725176845446.80E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
750269672rs1456893GArs1456893185873945.00E-09NA1.2NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1456893-AResearch Support, N.I.H., ExtramuralMeta-Analysis
750304461rs1456896CTrs1456896185873941.39E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
750304461rs1456896CTrs1456896211024631.00E-08NA1.14[1.09-1.20] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1456896-TResearch Support, N.I.H., ExtramuralMeta-Analysis
780279718rs3211830CTrs3211830176845443.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
781839553rs11978472ACrs11978472236659636.00E-06NA2[1.43-2.50]239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
788295001rs12531232TCrs12531232236659634.30E-05NA1.6NA983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers12531232-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
798887802rs10953286CTrs10953286205709664.40E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
7102471213rs10487283TCrs10487283176845448.60E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
7109782499rs1722052TGrs1722052236659634.10E-05NA1.67NA239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
7110442772rs1528039AGrs1528039176845449.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
7112718186rs2255323CTrs2255323224828048.86E-09NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
7113707787rs10500037TCrs10500037176845449.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
7114357543rs1869839AGrs1869839229366697.00E-06NA1.2[1.11-1.30] 1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
7118515456rs10500069AGrs10500069176845448.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
7125533006rs6947579GCrs6947579176845444.80E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
7125570097rs10487428ATrs10487428176845445.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
7148258048rs7807268GCrs7807268175543004.00E-06NA1.38[1.20-1.60]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7807268-GMulticenter StudyResearch Support, N.I.H., Extramural
7154402669rs1488927CGrs1488927176845446.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
84638706rs10503282AGrs10503282176845443.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
815013234rs10503536AGrs10503536176845449.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
817670196rs396462GCrs396462176845446.90E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
852820274rs11775611TCrs11775611178047894.07E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
859217726rs10504252ACrs10504252176845447.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
874007347rs12677663GTrs12677663224123882.00E-08NA1.15[1.04-1.28] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers12677663-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
878500065rs723510TCrs723510176845446.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
890875918rs7015630TCrs7015630231282331.00E-08NA1.08[1.03-1.12] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7015630-TResearch Support, N.I.H., ExtramuralMeta-Analysis
8101975479rs2386922TGrs2386922178047892.04E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
8102330393rs10505007AGrs10505007174357563.78E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
8106707739rs6469010TCrs6469010236659631.90E-05NA1.8[1.40-2.40]983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers6469010-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
8114799224rs2044999GArs2044999174357563.84E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
8117928825rs3020167CTrs3020167238507135.82E-05NA1.2[1.10-1.31]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3020167-TResearch Support, Non-U.S. Gov'tValidation Studies
8126534671rs921720AGrs921720185873942.78E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
8126537570rs4871611GArs4871611211024632.00E-12NA1.17[1.12-1.23] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4871611-AResearch Support, N.I.H., ExtramuralMeta-Analysis
8126540051rs1551398GArs1551398185873945.00E-09NA1.08NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1551398-AResearch Support, N.I.H., ExtramuralMeta-Analysis
8127092882rs1906493GTrs1906493224123883.00E-06NA1.19[1.09-1.28] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1906493-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
8129567181rs6651252TCrs6651252211024634.00E-18NA1.23[1.17-1.30]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6651252-TResearch Support, N.I.H., ExtramuralMeta-Analysis
8129567181rs6651252TCrs6651252231282331.00E-16NA1.19[1.13-1.25] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6651252-TResearch Support, N.I.H., ExtramuralMeta-Analysis
8138378521rs10505673CTrs10505673176845444.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC,T
94974441rs1327495GArs1327495232665588.59E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
94979730rs1887427AGrs1887427232665586.43E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
94981602rs10758669CArs10758669185873943.00E-09NA1.12NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10758669-CResearch Support, N.I.H., ExtramuralMeta-Analysis
94981602rs10758669CArs10758669211024631.00E-13NA1.18[1.13-1.23] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10758669-CResearch Support, N.I.H., ExtramuralMeta-Analysis
94985879rs2274471AGrs2274471232665585.00E-06NA1.27[1.15-1.41] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2274471-AResearch Support, Non-U.S. Gov'tComparative Study
94988761rs7849191CTrs7849191185873944.34E-08NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
919458939rs960908CTrs960908205709666.50E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
927201968rs1413829AGrs1413829176845446.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
929223296rs10813028CTrs10813028205709664.16E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
986707888rs7029403GArs7029403236659633.30E-05NA2[1.43-2.50]239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
989959601rs4878061GArs4878061174357564.64E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
993008041rs10821091CTrs10821091174357561.44E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
9104479480rs4743484CTrs4743484176845448.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9104536303rs4743487ACrs4743487176845442.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
9109819928rs4978664GArs4978664176845441.67E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
9115698346rs747066CTrs747066176845441.50E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117420132rs2274598AGrs2274598162217588.50E-05Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
9117444370rs1075371CArs1075371162217581.45E-04Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117483015rs10817669GArs10817669232665582.96E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117504798rs2068955AGrs2068955232665582.72E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117516418rs7038398CArs7038398232665582.80E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117521582rs12552933CTrs12552933232665583.76E-08NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117530319rs4978609AGrs4978609232665583.34E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117538334rs4574921CTrs4574921162217587.76E-11Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
9117538334rs4574921CTrs4574921232665581.83E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117545666rs6478106CTrs6478106162217587.76E-07Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117545666rs6478106CTrs6478106232665585.00E-46NA1.73[1.60-1.86] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6478106-TResearch Support, Non-U.S. Gov'tComparative Study
9117547772rs10114470TCrs10114470232665584.82E-11NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117551603rs10117785TArs10117785162217582.51E-12Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
9117552885rs3810936TCrs3810936162217583.89E-11Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117552885rs3810936TCrs3810936211024631.00E-15NA1.21[1.15-1.27]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3810936-CResearch Support, N.I.H., ExtramuralMeta-Analysis
9117553249rs4246905TCrs4246905162217583.02E-06Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
9117558703rs6478108CTrs6478108162217585.62E-14Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
9117558703rs6478108CTrs6478108232665581.53E-12NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117563687rs4372078TGrs4372078162217586.46E-10Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
9117566440rs4263839AGrs4263839185873943.00E-10NA1.22NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4263839-GResearch Support, N.I.H., ExtramuralMeta-Analysis
9117567013rs4979462CTrs4979462162217583.38E-13Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117568766rs6478109AGrs6478109162217581.17E-11Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
9117568766rs6478109AGrs6478109185873943.67E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
9117568766rs6478109AGrs6478109232665586.84E-12NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117569046rs7848647TCrs7848647162217584.43E-11Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117580914rs7869487CTrs7869487162217583.24E-11Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
9117592638rs2006996TCrs2006996232665581.22E-10NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117618309rs16931910ACrs16931910162217585.50E-08Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
9117627569rs7866342GTrs7866342232665582.69E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117630043rs4979467CTrs4979467232665586.72E-09NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117642418rs7863183TCrs7863183232665581.33E-07NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117645015rs7028891AGrs7028891232665581.30E-06NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117664172rs2974TCrs2974162217581.97E-07Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117664211rs2295800TCrs2295800162217583.06E-08Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
9117664211rs2295800TCrs2295800232665581.79E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117667443rs3181362TCrs3181362162217582.75E-04Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
9117667443rs3181362TCrs3181362232665586.38E-10NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117667937rs3181196GA,C,Trs3181196162217582.75E-06Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117669270rs3827818CTrs3827818162217585.62E-05Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
9117669299rs1322054AGrs1322054162217589.13E-09Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
9117669699rs3789882ATrs3789882162217584.45E-09Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
9117678236rs3789879TCrs3789879162217583.70E-09Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
9117679802rs1885383GArs1885383162217581.61E-09Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
9117690864rs2181032CTrs2181032162217584.37E-05Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117691364rs4978612TArs4978612162217585.50E-05Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
9117691558rs3181360CA,G,Trs3181360162217588.13E-05Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
9117691558rs3181360CA,G,Trs3181360232665587.94E-10NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117692344rs3181357GArs3181357162217582.88E-06Crohn's diseaseNANA94 Japanese CD patients; 752 Japanese controlsJapanese(846)ALL(846)ASN(846)ALL(846)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
9117694184rs3181348GArs3181348232665582.33E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117754106rs16932027CTrs16932027232665583.77E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9117757075rs17817825ACrs17817825232665585.34E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
9135974100rs886017GArs886017224828041.43E-05NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
9137506578rs11103429AGrs11103429236659636.00E-06NA3.6[2.10-6.30]239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers11103429-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
9139266496rs4077515CTrs4077515211024631.00E-36NA1.18[1.13-1.22]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4077515-TResearch Support, N.I.H., ExtramuralMeta-Analysis
9139266496rs4077515CTrs4077515229366694.00E-06NA1.29NA1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4077515-TResearch Support, Non-U.S. Gov'tG
9139396113rs11574906TArs11574906224828042.74E-07NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
103862542rs6601764CTrs6601764175543009.00E-06NA1.16[1.01-1.33]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers6601764-CMulticenter StudyResearch Support, N.I.H., Extramural
106102012rs12722489CTrs12722489211024633.00E-09NA1.11[1.05-1.16] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers12722489-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1013659738rs2478126ACrs2478126176845442.70E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1015821778rs10508494CGrs10508494176845448.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1020646439rs10508621CGrs10508621176845448.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1023665438rs1398024GTrs1398024187230194.00E-06NA1.23[1.04-1.45] 382 CD cases; 398 SA cases; 394 controlsNOPOP(1174)ALL(1174)NOPOP(1174)ALL(1174)Crohn's disease and sarcoidosis (combined)HPOID:0100280Crohn's diseaseDOID:8778DOID:13402Crohn's diseaseskin sarcoidosisD003424Crohn DiseaseNANAEnteritisIntestinal diseaseSarcoidosis
1035287650rs17582416TGrs17582416185873942.00E-09NA1.16NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers17582416-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1035535695rs12242110AGrs12242110211024631.00E-09NA1.15[1.10-1.20] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers12242110-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1035549257rs3936503GArs3936503185873948.04E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1050294670rs4317904GArs4317904212980272.80E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
1052010708rs10508921CTrs10508921176845444.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1059913151rs1819658CTrs1819658211024639.00E-17NA1.19[1.13-1.25]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1819658-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1061713218rs7094419TCrs7094419232665581.82E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1064414060rs7071642GArs7071642224828043.41E-08NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1064415184rs7076156AGrs7076156224123887.00E-09NA1.19[1.10-1.30] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7076156-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1064438486rs10995271GCrs10995271185873944.00E-20NA1.25NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10995271-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1064445564rs10761659AGrs10761659175543002.00E-06NA1.23[1.05-1.45]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10761659-GMulticenter StudyResearch Support, N.I.H., Extramural
1064445564rs10761659AGrs10761659211024634.00E-22NA1.23[1.18-1.29]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10761659-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1064445564rs10761659AGrs10761659229366695.00E-06NA1.28NA1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10761659-GResearch Support, Non-U.S. Gov'tA
1064466802rs224135AGrs224135232665582.84E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1064470675rs224136CTrs224136174357561.00E-10NA1.67NA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1075632760rs2675671CTrs2675671224828043.89E-06NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1075654931rs2688610GArs2688610185873943.32E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1076617479rs951308TCrs951308176845446.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1076670311rs7092435GCrs7092435176845441.90E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1077029174rs10509357AGrs10509357176845441.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1081032885rs1250544GArs1250544224828047.00E-14same-effect analysis1.16NA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1081060317rs1250550CArs1250550211024631.00E-30NA1.19[1.15-1.23]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1250550-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1091414563rs78765440TCrs78765440232665585.40E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1098988469rs793515ACrs793515176845442.50E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
10100383999rs483952CG,Trs483952176845448.73E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
10101284237rs4409764TGrs4409764211024632.00E-20NA1.22[1.17-1.27]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4409764-TResearch Support, N.I.H., ExtramuralMeta-Analysis
10101287764rs10883365GArs10883365175542614.00E-10NA1.18[1.05-1.32]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
10101287764rs10883365GArs10883365175543006.00E-08NA1.2[1.03-1.39]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10883365-GMulticenter StudyResearch Support, N.I.H., Extramural
10101291593rs11190140TCrs11190140185873943.00E-16NA1.2NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11190140-TResearch Support, N.I.H., ExtramuralMeta-Analysis
10101292390rs11190141CTrs11190141224123885.00E-07NA1.34[1.25-1.43] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11190141-CResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
10108332996rs12415344GArs12415344224828049.38E-05NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
10112186148rs11195128CTrs11195128238507132.00E-10NA1.42[1.28-1.58]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11195128-TResearch Support, Non-U.S. Gov'tValidation Studies
10117350004rs10509992AGrs10509992176845448.67E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
10117350297rs2804200CGrs2804200176845442.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
10117350560rs10509991AGrs10509991176845443.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
10117358809rs1590736AGrs1590736176845441.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
10117358919rs1590734GCrs1590734176845445.57E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
10121105311rs10886462AGrs10886462178047899.55E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
10121859814rs1467785TCrs1467785205709668.56E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
10133172119rs10734105GArs10734105224123883.00E-08NA1.27[1.10-1.43] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers10734105-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
10133231622rs3922590CTrs3922590176845445.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1114070567rs1919295CTrs1919295205709665.26E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1120698929rs1793004CGrs1793004176845443.00E-06NA1.3[1.12-1.52]393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1120700775rs951199CGrs951199176845448.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1120876346rs12293297GArs12293297176845449.50E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1135364435rs3847621GArs3847621176845449.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA,G
1135998208rs10836477TGrs10836477224828044.12E-06NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1142996387rs10501292AGrs10501292176845448.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1157203009rs11229030CTrs11229030224123888.00E-09NA1.15[1.10-1.39] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11229030-CResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1161557803rs102275TCrs102275211024632.00E-11NA1.08[1.04-1.12]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers102275-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1164097233rs694739AGrs694739211024636.00E-10NA1.1[1.05-1.16]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers694739-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1164150370rs559928TCrs559928185873947.44E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1164210652rs596308GArs596308185873943.45E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1172184591rs11235508CTrs11235508236659631.50E-05NA2.2NA239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers11235508-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1172184591rs11235508CTrs11235508236659632.50E-05NA1.9[1.40-2.50]983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers11235508-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1172533536rs11235604CTrs11235604238507132.44E-12NA1.61[1.41-1.83]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11235604-TResearch Support, Non-U.S. Gov'tValidation Studies
1172670900rs72981516TGrs72981516232665584.00E-07NA1.28[1.27-1.29] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers72981516-TResearch Support, Non-U.S. Gov'tComparative Study
1172863697rs11235667AGrs11235667238507137.00E-09NA1.46[1.28-1.65]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11235667-GResearch Support, Non-U.S. Gov'tValidation Studies
1174852100rs2712800TGrs2712800174357562.38E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1176301316rs7927894CTrs7927894185873941.00E-09NA1.16NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7927894-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1176301375rs7927997CTrs7927997211024636.00E-13NA1.17[1.12-1.22] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7927997-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1176339953rs11236811GArs11236811232665587.61E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1176975467rs1793483TCrs1793483176845444.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1188638182rs549700CTrs549700176845447.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1190262683rs10501720ATrs10501720176845442.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1192865007rs12576495TCrs12576495178047891.00E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1195840120rs10501843GArs10501843176845441.80E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1195840436rs1074742AGrs1074742176845441.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
11114093055rs3781990CTrs3781990205709667.80E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
11114999873rs2513676AGrs2513676205709662.30E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
122481936rs886898TCrs886898174357561.93E-05NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1221014139rs3764008CGrs3764008176845443.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1221014163rs3764007TArs3764007176845445.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1228491157rs2169755CGrs2169755212980276.45E-05NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
1228521109rs1586868CTrs1586868212980277.36E-05NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
1228534569rs1257741GCrs1257741212980275.62E-05NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
1228605426rs10771427GArs10771427212980275.72E-05NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
1240601940rs11175593CTrs11175593185873943.00E-10NA1.54NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11175593-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1240792300rs11564258GArs11564258211024636.00E-21NA1.74[1.55-1.95]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11564258-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1243149010rs11181674ATrs11181674178047898.71E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1243714537rs2134066AGrs2134066176845448.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1246043613rs10492248TCrs10492248176845449.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1251087857rs10506296CGrs10506296176845449.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1256439209rs12580100AGrs12580100224828046.18E-07NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1259773458rs1996199AGrs1996199185873943.97E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1274874472rs10785122AGrs10785122205709666.16E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1296267298rs10507063GCrs10507063176845441.19E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
12101530109rs823559AGrs823559236659634.80E-05NA2[1.40-2.80]983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers823559-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
12102985749rs1463446AGrs1463446176845445.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
12124583446rs902169GArs902169205709669.90E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1320939236rs1105267GArs1105267170682235.12E-10NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralC
1324318963rs1536299ACrs1536299176845446.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1324531398rs2765122GArs2765122236659633.80E-05NA2NA983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1336848187rs912927TCrs912927205709668.20E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1339445743rs9548517GArs9548517236659633.00E-05NA1.8[1.40-2.40]983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers9548517-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1341416221rs7992208TCrs7992208232665581.09E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341427029rs59597769TCrs59597769232665581.66E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341427506rs77419885CTrs77419885232665582.00E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341437926rs7339089CTrs7339089232665581.62E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341438217rs79487860GArs79487860232665582.71E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341470342rs7329474CTrs7329474232665583.32E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341487686rs57088152TCrs57088152232665581.75E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341501643rs9594460CArs9594460232665583.32E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341510339rs77419017GArs77419017232665581.39E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341522272rs75719223TGrs75719223232665581.51E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341526350rs60129138CTrs60129138232665581.96E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341539817rs17630801ACrs17630801232665581.59E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341547143rs77553977TCrs77553977232665585.93E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341552738rs9532692GArs9532692232665582.63E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341555724rs78076494GArs78076494232665581.48E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341557118rs57668933TCrs57668933232665582.75E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341558110rs7329174AGrs7329174232665588.00E-09NA1.27[1.17-1.38] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers7329174-GResearch Support, Non-U.S. Gov'tComparative Study
1341562860rs12585650CArs12585650232665581.56E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341563902rs78053745TCrs78053745232665582.86E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341564287rs59691646ACrs59691646232665582.53E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341568872rs80022860GArs80022860232665582.17E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341575804rs74674762TCrs74674762232665582.86E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341579868rs7335629TCrs7335629232665588.39E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341583941rs12584853CTrs12584853232665586.96E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341585055rs74757048TCrs74757048232665581.81E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341588832rs4264266GTrs4264266232665581.03E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1341602462rs61300271TCrs61300271232665584.81E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1343052880rs2062305GArs2062305211024635.00E-10NA1.1[1.05-1.15]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2062305-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1344457925rs3764147AGrs3764147185873942.00E-13NA1.25NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3764147-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1344457925rs3764147AGrs3764147211024631.00E-10NA1.17[1.12-1.23] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3764147-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1344457925rs3764147AGrs3764147231282332.00E-21NA1.16[1.11-1.20] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3764147-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1344599789rs9562532GArs9562532185873941.44E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1359844496rs1998828GTrs1998828236659632.70E-05NA1.6NA983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers1998828-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1361188132rs995085CTrs995085205709668.00E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1366536090rs17837226CTrs17837226178047894.37E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1369763228rs8000906CTrs8000906176845445.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1375331093rs11617463CArs11617463174357561.62E-05NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1379744855rs605216GTrs605216176845442.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1394906103rs1333261CTrs1333261176845441.80E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1396234753rs7324781CTrs7324781176845444.37E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1425616536rs9323605GArs9323605176845448.10E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1432728233rs6571501CArs6571501205709667.46E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1433591105rs8005131GCrs8005131176845444.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1438185661rs4901140AGrs4901140236659631.90E-05NA1.7[1.40-2.30]983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers4901140-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1452413573rs10498440TCrs10498440176845442.50E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1456454074rs1188157CTrs1188157174357561.58E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1469210199rs4902642GArs4902642211024632.00E-10NA1.07[1.11-1.04]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4902642-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1476001394rs7161377TCrs7161377185873942.25E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1476031313rs7159570AGrs7159570236659631.80E-05NA2[1.11-2.50]239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1488472595rs8005161CTrs8005161211024634.00E-18NA1.23[1.16-1.31]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers8005161-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1497857732rs8011773CTrs8011773176845445.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1499375321rs200354GTrs200354176845442.22E-06NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
14101539131rs2295655GArs2295655236659633.60E-05NA1.8[1.30-2.30]239 European ancestry cases that required surgery within 5 year; 375 European ancestry cases that did not require surgery within 5 yearsEuropean(614)ALL(614)EUR(614)ALL(614)Crohn's disease (need for surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers2295655-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1524050205rs10519449TCrs10519449176845448.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1538899190rs16967103TCrs16967103231282334.00E-09NA1.09[1.04-1.13] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers16967103-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1540558087rs2016902GArs2016902224828041.42E-06NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1556701500rs2414476CArs2414476178047898.71E-09NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1567442596rs17293632CTrs17293632211024633.00E-19NA1.12[1.07-1.16]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers17293632-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1585581389rs289386CTrs289386176845446.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1586268672rs471073CArs471073236659631.70E-05NA1.8[1.40-2.30]983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers471073-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1586360145rs4842903CArs4842903205709669.96E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1592720600rs10520704AGrs10520704176845448.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1595927728rs10520778CArs10520778176845449.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
163203335rs224188TCrs224188174478422.00E-04NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1611347858rs4780355TCrs4780355224828041.00E-13same-effect analysis1.16NA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1617912586rs1994893TCrs1994893176845449.20E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1628490517rs151181TCrs151181211024632.00E-11NA1.07[1.03-1.12]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers151181-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1650443200rs4369662TCrs4369662178047894.90E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650445412rs4483840GTrs4483840178047894.70E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650464110rs1861543CTrs1861543178047895.11E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650508101rs6500315AGrs6500315178047891.04E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650525105rs1592473TGrs1592473178047893.85E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650536826rs12149258AGrs12149258178047897.73E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650565970rs1990623AGrs1990623178047893.16E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650627378rs4785220TCrs4785220178047892.31E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650660764rs8046845GArs8046845178047894.33E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650662844rs1558663GArs1558663178047891.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650665089rs11640716TGrs11640716178047894.97E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650666566rs7198686TCrs7198686178047897.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650668426rs12913TCrs12913178047894.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650670182rs745230GCrs745230178047894.30E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650671721rs12924696GArs12924696178047891.97E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650673651rs749985TCrs749985178047891.42E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650679315rs9926095ACrs9926095178047896.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650686557rs7186163ACrs7186163178047893.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650687673rs8050932CTrs8050932178047891.58E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650692364rs1109863GArs1109863178047893.16E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650709723rs6596GArs6596178047894.71E-29NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650714029rs7202124GArs7202124178047892.38E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650715185rs2066848GArs2066848178047891.51E-09NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650718041rs8062727GArs8062727178047897.67E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650719674rs1420685TCrs1420685178047897.05E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650720917rs2004804GArs2004804178047895.11E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650723074rs1981760CTrs1981760178047896.12E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650725193rs7194886CTrs7194886178047892.93E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650730446rs4785224GArs4785224178047891.01E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650733374rs2076753GTrs2076753178047898.63E-23NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650733969rs2111235AGrs2111235178047894.16E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650737980rs8057341AGrs8057341178047892.14E-09NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650739582rs17221417CGrs17221417175543004.00E-11NA1.29[1.13-1.46]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers17221417-GMulticenter StudyResearch Support, N.I.H., Extramural
1650739582rs17221417CGrs17221417178047894.11E-25NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650741462rs17312836ACrs17312836178047894.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650743331rs11647841GArs11647841178047891.55E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650744624rs2066842CTrs2066842178047893.49E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650745199rs2066843CTrs2066843170682232.86E-09NANANA547 cases; 548 controlsNOPOP(1095)ALL(1095)NOPOP(1095)ALL(1095)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralC
1650745926rs2066844CTrs2066844176845441.29E-18NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650745926rs2066844CTrs2066844178047892.61E-10NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650747704rs17313265CTrs17313265178047897.31E-29NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650751175rs751271TGrs751271178047895.26E-11NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650753424rs7203691GArs7203691178047891.37E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650755709rs10521209TGrs10521209176845448.65E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650756540rs2066845GC,Trs2066845176845447.44E-10NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650756540rs2066845GC,Trs2066845178047891.00E-45NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650756540rs2066845GC,Trs2066845185873944.62E-08NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1650756774rs5743289CG,Trs5743289174478421.00E-06NANANA547 cases; 928 controlsNOPOP(1475)ALL(1475)NOPOP(1475)ALL(1475)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650756774rs5743289CG,Trs5743289178047896.00E-17NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650756881rs2076756AGrs2076756174357567.00E-14NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1650756881rs2076756AGrs2076756176845441.00E-21NA1.71[1.42-2.05]393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650756881rs2076756AGrs2076756178047891.00E-09NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650756881rs2076756AGrs2076756211024634.00E-69NA1.53[1.46-1.60]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2076756-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1650756881rs2076756AGrs2076756224123881.00E-37NA1.66[1.48-1.88]737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2076756-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1650756881rs2076756AGrs2076756229366693.00E-10NA1.46NA1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2076756-GResearch Support, Non-U.S. Gov'tA
1650757276rs5743291GArs5743291178047891.00E-20NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650758849rs749910GArs749910178047891.84E-31NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650763778rs199883290GCrs2066847176845442.51E-49NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650763778rs199883290GCrs2066847185873943.00E-24NA3.99NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2066847-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1650763778rs199883290GCrs2066847205709662.00E-15NA1.62[1.42-1.86]896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1650763778rs199883290GCrs2066847231282336.00E-209NA3.1[1.50-1.62] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2066847-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1650763778rs2066847GGCrs2066847176845442.51E-49NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650763778rs2066847GGCrs2066847185873943.00E-24NA3.99NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2066847-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1650763778rs2066847GGCrs2066847205709662.00E-15NA1.62[1.42-1.86]896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1650763778rs2066847GGCrs2066847231282336.00E-209NA3.1[1.50-1.62] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2066847-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1650763778rs540973741GGCrs2066847176845442.51E-49NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650763778rs540973741GGCrs2066847185873943.00E-24NA3.99NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2066847-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1650763778rs540973741GGCrs2066847205709662.00E-15NA1.62[1.42-1.86]896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1650763778rs540973741GGCrs2066847231282336.00E-209NA3.1[1.50-1.62] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2066847-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1650763778rs5743293GGCrs2066847176845442.51E-49NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650763778rs5743293GGCrs2066847185873943.00E-24NA3.99NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2066847-CResearch Support, N.I.H., ExtramuralMeta-Analysis
1650763778rs5743293GGCrs2066847205709662.00E-15NA1.62[1.42-1.86]896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1650763778rs5743293GGCrs2066847231282336.00E-209NA3.1[1.50-1.62] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2066847-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1650766127rs3135499ACrs3135499178047891.62E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650767647rs8056611AGrs8056611178047896.68E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650775745rs751919TGrs751919178047892.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650781802rs8060598TCrs8060598178047893.16E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650787483rs7342715AGrs7342715178047891.26E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650791250rs3135503TGrs3135503178047893.16E-08NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650808726rs6500331GArs6500331178047891.89E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650817932rs8062540AGrs8062540178047899.73E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650819910rs2111435CTrs2111435178047892.60E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650822964rs4785226ACrs4785226178047897.50E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650827601rs2302759AGrs2302759178047897.00E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650829853rs2160683ATrs2160683178047892.27E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1650839648rs1861762TCrs1861762178047892.27E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650842077rs4785452TCrs4785452178047891.79E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650848973rs12922698CTrs12922698178047894.26E-09NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650916464rs2029923CArs2029923178047893.63E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650949161rs17226979AGrs17226979178047896.18E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650973078rs9935378CTrs9935378178047891.18E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650974725rs4785482CTrs4785482178047891.09E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650976307rs17325379ATrs17325379178047892.13E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1650978048rs1872679TGrs1872679178047898.49E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650979745rs4785483GCrs4785483178047899.86E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1650984731rs6500350CGrs6500350178047893.66E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650988142rs4785484GCrs4785484178047892.02E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650990540rs2129247CTrs2129247178047893.44E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1650999201rs1528602TCrs1528602178047891.82E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1651007618rs2129250GArs2129250178047895.70E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1651009198rs16949179TCrs16949179178047897.36E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1651068059rs7191446AGrs7191446178047895.78E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1651083636rs8060595AGrs8060595178047892.13E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1653253710rs58474046TCrs58474046238507132.84E-04NA1.19[1.08-1.31]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers58474046-CResearch Support, Non-U.S. Gov'tValidation Studies
1667971380rs11574514CTrs11574514224123882.00E-07NA1.44[1.35-1.52] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11574514-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1675167579rs7195303GArs7195303236659639.00E-06NA2.1[1.50-2.80]983 European ancestry casesEuropean(983)ALL(983)EUR(983)ALL(983)Crohn's disease (time to surgery)HPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseNANANANAEnteritisIntestinal diseasers7195303-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1684248757rs40254AGrs40254212980272.97E-05NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
1685139173rs8050910GTrs8050910174357569.55E-06NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1685987998rs10863202AGrs10863202185873941.40E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1725843643rs2945412GArs2945412231282339.00E-17NA1.14[1.10-1.18] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2945412-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1725870542rs2948529CTrs2948529178047896.57E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1725872185rs2948527TCrs2948527178047895.85E-04NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1725983153rs4794986GArs4794986178047896.92E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA,G
1726103034rs4796052CTrs4796052178047897.34E-04NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1726545488rs12452097CArs12452097178047891.10E-04NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1726549716rs4435306TGrs4435306178047895.15E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1732587725rs991804CTrs991804185873945.34E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1732593665rs3091315AGrs3091315211024632.00E-13NA1.2[1.14-1.26]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3091315-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1732593974rs3091316GArs3091316224123884.00E-08NA1.14[1.03-1.27] 737 Ashkenazi Jewish cases; 2,257 Ashkenazi Jewish controlsAshkenazi Jewish(2994)ALL(2994)MEA(2994)ALL(2994)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers3091316-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1738040763rs2872507GArs2872507185873945.00E-09NA1.12NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2872507-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1738040763rs2872507GArs2872507211024632.00E-09NA1.14[1.09-1.19] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2872507-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1738062196rs2305480GArs2305480185873945.45E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1740494902rs8069645AGrs8069645232665582.49E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1740499533rs6503695TCrs6503695232665582.49E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1740507980rs9891119ACrs9891119232665582.00E-15NA1.37[1.27-1.48] 372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers9891119-AResearch Support, Non-U.S. Gov'tComparative Study
1740514201rs744166AGrs744166185873947.00E-12NA1.18NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers744166-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1740514201rs744166AGrs744166232665581.69E-05NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1740552794rs2883456CTrs2883456232665581.42E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1740566240rs1968866TCrs1968866232665586.96E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1740570602rs12948909ACrs12948909185873947.10E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1740570772rs11871801ACrs11871801211024633.00E-08NA1.15[1.10-1.21] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers11871801-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1740582296rs1905339TCrs1905339232665583.59E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
1741983498rs231480GArs231480178047899.04E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1757943115rs2645482TGrs2645482178047895.57E-04NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1757963537rs1292053AGrs1292053178047897.11E-04NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1758828624rs8077981TCrs8077981178047895.13E-07NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1759158243rs6504016GArs6504016178047893.99E-05NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1759245274rs4968535TCrs4968535176845444.50E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
18631435rs10502288GArs10502288176845442.50E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
188627595rs9304017AGrs9304017176845448.40E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
1812779947rs2542151GTrs2542151175542613.00E-08 1.15[1.00-1.32] 1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1812779947rs2542151GTrs2542151175543002.00E-07NA1.3[1.14-1.48]1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2542151-GMulticenter StudyResearch Support, N.I.H., Extramural
1812779947rs2542151GTrs2542151185873945.00E-17NA1.35NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2542151-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1812779947rs2542151GTrs2542151212980271.19E-11NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
1812809340rs1893217AGrs1893217185873947.05E-16NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1812809340rs1893217AGrs1893217211024631.00E-14NA1.25[1.18-1.32] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1893217-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1812809340rs1893217AGrs1893217212980276.54E-11NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
1812847136rs657555CTrs657555212980273.02E-09NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
1813503887rs1559865GTrs1559865176845441.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
1819673331rs8098673ACrs8098673185873941.44E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1842800148rs10502861CTrs10502861176845445.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1847580051rs2852095GArs2852095176845449.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
1855903021rs158865CTrs158865185873941.97E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1856567906rs937815GTrs937815174357563.25E-05NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
1869154730rs10514013AGrs10514013176845446.30E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
191123378rs4807569ACrs4807569185873941.06E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
191124031rs2024092GArs2024092185873941.80E-10NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
191124031rs2024092GArs2024092231282338.00E-22NA1.16[1.11-1.20] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2024092-AResearch Support, N.I.H., ExtramuralMeta-Analysis
191124835rs740495AGrs740495211024638.00E-12NA1.16[1.10-1.21] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers740495-GResearch Support, N.I.H., ExtramuralMeta-Analysis
191312728rs10405308GArs10405308224828041.81E-07NANANA2,529 European ancestry psoriasis cases; 2,142 European ancestry Crohn's disease cases; 10,460 European ancestry controlsEuropean(15131)ALL(15131)EUR(15131)ALL(15131)Crohn's disease and psoriasisHPOID:0100280Crohn's diseaseDOID:8778DOID:8893Crohn's diseasepsoriasisD011565PsoriasisEFOID:0000676crohn's diseasePsoriasisEnteritisIntestinal disease
1910469975rs12720356ACrs12720356211024631.00E-12NA1.12[1.06-1.19]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers12720356-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1918439383rs12985909CTrs12985909185873947.54E-07NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
1933757062rs736289TCrs736289211024639.00E-09NA1.06[1.02-1.11] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers736289-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1946849806rs4802307GTrs4802307231282332.00E-10NA1.1[1.06-1.14] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4802307-GResearch Support, N.I.H., ExtramuralMeta-Analysis
1948719688rs2009530CArs2009530176845444.92E-06NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
1949206172rs516246CTrs516246231282331.00E-15NA1.11[1.07-1.14] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers516246-TResearch Support, N.I.H., ExtramuralMeta-Analysis
1949208865rs504963GArs504963205709662.00E-08NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers504963-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1949214274rs281379GArs281379211024637.00E-12NA1.07[1.04-1.11]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers281379-AResearch Support, N.I.H., ExtramuralMeta-Analysis
1955682046rs3859540CTrs3859540176845446.18E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
206089513rs6516104CTrs6516104212980276.19E-04NANANA3,230 European ancestry Crohn's disease cases; 4,829 European ancestry Crohn's disease controls; 768 European ancestry celiac disease cases; 1,422 European ancestry celiac disease controlsEuropean(10249)ALL(10249)EUR(10249)ALL(10249)Crohn's disease and Celiac diseaseHPOID:0100280Crohn's diseaseDOID:8778DOID:10608Crohn's diseaseceliac diseaseD002446Celiac DiseaseEFOID:0000384celiac diseaseCeliac diseaseEnteritisIntestinal disease
2010692559rs973542GArs973542176845442.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
2010692989rs6077888CTrs6077888176845442.70E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
2014706879rs6074780TArs6074780176845447.12E-05NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
2014849853rs10485515GArs10485515176845447.80E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
2046340506rs4810663CTrs4810663174357563.45E-04NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
2047063526rs7263053CTrs7263053176845443.90E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
2047063883rs6122682TCrs6122682176845447.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
2057917689rs6128541TCrs6128541185873941.80E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2062327582rs2297441GArs2297441185873941.30E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2062349586rs4809330AGrs4809330211024633.00E-15NA1.12[1.06-1.18]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4809330-GResearch Support, N.I.H., ExtramuralMeta-Analysis
2062349625rs2738758CGrs2738758185873942.66E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2116805220rs1736135TCrs1736135185873947.00E-09NA1.18NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1736135-TResearch Support, N.I.H., ExtramuralMeta-Analysis
2116812552rs1736020CArs1736020185873943.36E-08NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2116812552rs1736020CArs1736020211024639.00E-12NA1.16[1.11-1.21] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers1736020-CResearch Support, N.I.H., ExtramuralMeta-Analysis
2128745816rs2167597CTrs2167597205709668.96E-05NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2130549361rs2832238GTrs2832238176845447.60E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
2134776695rs2284553AGrs2284553231282332.00E-16NA1.12[1.09-1.16] Up to 12,924 European ancestry cases; up to 21,442 European ancestry controls European(34366)ALL(34366)EUR(34366)ALL(34366)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2284553-GResearch Support, N.I.H., ExtramuralMeta-Analysis
2134796886rs2834215AGrs2834215229366693.00E-07NA1.22[1.12-1.32] 1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tG
2140291740rs2836754TCrs2836754175542615.00E-07 1.15[1.03-1.28] 1,748 cases; 2,938 controlsNOPOP(4686)ALL(4686)NOPOP(4686)ALL(4686)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
2142019009rs2837758CTrs2837758176845449.50E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tT
2145611950rs743479CTrs743479185873944.30E-09NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2145615023rs2838519GArs2838519211024632.00E-14NA1.18[1.13-1.23] 6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2838519-GResearch Support, N.I.H., ExtramuralMeta-Analysis
2145615561rs762421GArs762421185873941.00E-09NA1.13NA3,230 European ancestry cases; 4,829 European ancestry controlsEuropean(8059)ALL(8059)EUR(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers762421-GResearch Support, N.I.H., ExtramuralMeta-Analysis
2221928641rs181359GArs181359211024635.00E-16NA1.1[1.06-1.15]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers181359-TResearch Support, N.I.H., ExtramuralMeta-Analysis
2221939675rs5754217GTrs5754217185873946.26E-06NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2221956653rs2283790AGrs2283790185873944.55E-05NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
2222726968rs10483112CTrs10483112176845443.90E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tNA
2227747270rs569626GArs569626176845448.00E-04NANANA393 cases; 399 controlsNOPOP(792)ALL(792)NOPOP(792)ALL(792)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tA
2230388758rs737909TGrs737909232665583.59E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
2230390990rs3788423TCrs3788423232665583.59E-04NANANA372 Japanese ancestry cases; 3,389 Japanese ancestry controlsJapanese(3761)ALL(3761)ASN(3761)ALL(3761)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tComparative Study
2230592487rs713875CGrs713875211024637.00E-12NA1.08[1.04-1.13]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers713875-CResearch Support, N.I.H., ExtramuralMeta-Analysis
2237258503rs4821544TCrs4821544174357561.75E-05NANANA946 cases; 977 controlsNOPOP(1923)ALL(1923)NOPOP(1923)ALL(1923)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralComparative Study
2237308785rs4821558TCrs4821558238507134.80E-04NA1.16[1.07-1.27]532 Korean ancestry cases; 733 Korean ancestry controlsKorean(1265)ALL(1265)ASN(1265)ALL(1265)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4821558-CResearch Support, Non-U.S. Gov'tValidation Studies
2239659773rs2413583CTrs2413583211024631.00E-26NA1.23[1.17-1.29]6,333 European ancestry cases; 15,056 European ancestry controlsEuropean(21389)ALL(21389)EUR(21389)ALL(21389)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers2413583-CResearch Support, N.I.H., ExtramuralMeta-Analysis
2239812986rs6001585CArs6001585205709666.00E-06NANANA896 European ancestry cases; 3,204 European ancestry controlsEuropean(4100)ALL(4100)EUR(4100)ALL(4100)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2241431342rs4820425CA,G,Trs4820425229366693.00E-08NA1.27[1.17-1.38] 1,277 European ancestry cases; 1,488 European ancestry controlsEuropean(2765)ALL(2765)EUR(2765)ALL(2765)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseasers4820425-AResearch Support, Non-U.S. Gov'tC
X34657756rs6632039GTrs6632039178047896.03E-06NANANA382 triosNOPOP(382)ALL(382)NOPOP(382)ALL(382)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, Non-U.S. Gov'tC
X126902497rs226534AGrs226534185873942.23E-20NANANA3,230 cases; 4,829 controlsNOPOP(8059)ALL(8059)NOPOP(8059)ALL(8059)Crohn's diseaseHPOID:0100280Crohn's diseaseDOID:8778Crohn's diseaseD003424Crohn DiseaseEFOID:0000384crohn's diseaseEnteritisIntestinal diseaseNAResearch Support, N.I.H., ExtramuralMeta-Analysis
Mapped by lexical matching(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0000010Recurrent urinary tract infectionsMP:0003617urinary bladder hypoplasia;HP:0008046Abnormality of the retinal vasculature
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0000010Recurrent urinary tract infectionsMP:0003257abnormal abdominal wall morphology;HP:0002586Peritonitis
Chemical(Total Drugs:8)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0010346acetaminophenD000082103-90-2crohn diseaseMESH:D003424therapeutic21127120
C0010346ampicillinD00066769-53-4crohn diseaseMESH:D003424therapeutic18319500
C0010346aztreonamD00139878110-38-0crohn diseaseMESH:D003424therapeutic18319500
C0010346chlordiazepoxideD00270758-25-3crohn diseaseMESH:D003424therapeutic18711101
C0010346ciprofloxacinD00293985721-33-1crohn diseaseMESH:D003424therapeutic12399240
C0010346linezolidD000069349-crohn diseaseMESH:D003424therapeutic18319500
C0010346methotrexateD0087271959/5/2crohn diseaseMESH:D003424therapeutic10592889
C0010346thalidomideD01379250-35-1crohn diseaseMESH:D003424therapeutic11339241
FDA approved drug and dosage information(Total Drugs:12)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D003424zyvoxlinezolid400MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsTABLET;ORALDiscontinuedNoneYesNo
MESH:D003424zyvoxlinezolid200MG/100ML (2MG/ML)SOLUTION;IV (INFUSION)PrescriptionAPYesNo
MESH:D003424zyvoxlinezolid100MG/5MLFOR SUSPENSION;ORALPrescriptionABYesYes
MESH:D003424zyvoxlinezolid400MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsTABLET;ORALDiscontinuedNoneYesNo
MESH:D003424zyvoxlinezolid200MG/100ML (2MG/ML)SOLUTION;IV (INFUSION)PrescriptionAPYesNo
MESH:D003424zyvoxlinezolid100MG/5MLFOR SUSPENSION;ORALPrescriptionABYesYes
MESH:D003424ciprociprofloxacin400MG/40ML (10MG/ML)INJECTABLE;INJECTIONDiscontinuedNoneYesNo
MESH:D003424ciprociprofloxacin250MG/5MLFOR SUSPENSION;ORALPrescriptionABYesNo
MESH:D003424ofirmevacetaminophen1GM/100ML (10MG/ML)SOLUTION;IV (INFUSION)PrescriptionAPYesYes
MESH:D003424ofirmevacetaminophen1GM/100ML (10MG/ML)SOLUTION;IV (INFUSION)PrescriptionAPYesYes
MESH:D003424acetaminophenacetaminophen650MGSUPPOSITORY;RECTALOver-the-counterNoneYesYes
MESH:D003424acetaminophenacetaminophen650MGSUPPOSITORY;RECTALOver-the-counterNoneYesYes
FDA labeling changes(Total Drugs:12)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D00342412/19/2002zyvoxlinezolidNosocomial pneumonia, community-acquired pneumonia, complicated and uncomplicated skin and skin structure infections, and vancomycin-resistant infections caused by susceptible strainsExtended age range down to birth for nosocomial pneumonia, community-acquired pneumonia, complicated skin and skin structure infections and vancomycin-resistant infections. Safety and efficacy extrapolated from studies in adults and supported by PK and comparator-controlled studies in patients from birth to 11 years Extended age range down to 5 years of age for uncomplicated skin and skin structure infections based upon a comparator-controlled study in 5 to 17 year olds Clearance of linezolid varies as a function of age; As age of pediatric patients increases, clearance gradually decreases, and by adolescence mean clearance values approach those observed in adults Pediatric patients exhibit wider variability in clearance and systemic exposure (AUC) compared with adults New every 8 hours dosing regimen for pediatric patients birth to 11 years of age and every 12 hours dosing regimen for pediatric patients 12 years and older Information on PK parameters, AE profile, laboratory changes, dosing, and clinical studiesLabelingB---Pfizer11/2/2005FALSE'
MESH:D00342412/19/2002zyvoxlinezolidNosocomial pneumonia, community-acquired pneumonia, complicated and uncomplicated skin and skin structure infections, and vancomycin-resistant infections caused by susceptible strainsExtended age range down to birth for nosocomial pneumonia, community-acquired pneumonia, complicated skin and skin structure infections and vancomycin-resistant infections. Safety and efficacy extrapolated from studies in adults and supported by PK and comparator-controlled studies in patients from birth to 11 years Extended age range down to 5 years of age for uncomplicated skin and skin structure infections based upon a comparator-controlled study in 5 to 17 year olds Clearance of linezolid varies as a function of age; As age of pediatric patients increases, clearance gradually decreases, and by adolescence mean clearance values approach those observed in adults Pediatric patients exhibit wider variability in clearance and systemic exposure (AUC) compared with adults New every 8 hours dosing regimen for pediatric patients birth to 11 years of age and every 12 hours dosing regimen for pediatric patients 12 years and older Information on PK parameters, AE profile, laboratory changes, dosing, and clinical studiesLabelingB---Pfizer11/2/2005FALSE'
MESH:D00342412/19/2002zyvoxlinezolidNosocomial pneumonia, community-acquired pneumonia, complicated and uncomplicated skin and skin structure infections, and vancomycin-resistant infections caused by susceptible strainsExtended age range down to birth for nosocomial pneumonia, community-acquired pneumonia, complicated skin and skin structure infections and vancomycin-resistant infections. Safety and efficacy extrapolated from studies in adults and supported by PK and comparator-controlled studies in patients from birth to 11 years Extended age range down to 5 years of age for uncomplicated skin and skin structure infections based upon a comparator-controlled study in 5 to 17 year olds Clearance of linezolid varies as a function of age; As age of pediatric patients increases, clearance gradually decreases, and by adolescence mean clearance values approach those observed in adults Pediatric patients exhibit wider variability in clearance and systemic exposure (AUC) compared with adults New every 8 hours dosing regimen for pediatric patients birth to 11 years of age and every 12 hours dosing regimen for pediatric patients 12 years and older Information on PK parameters, AE profile, laboratory changes, dosing, and clinical studiesLabelingB---Pfizer11/2/2005FALSE'
MESH:D00342412/5/2005zyvoxlinezolidCentral nervous system infectionsPK data in pediatric patients with ventriculoperitoneal shunts showed variable cerebrospinal fluid (CSF) concentrations; therapeutic concentrations were not consistently achieved or maintained in the CSF Use of linezolid for the empiric treatment of pediatric patients with central nervous system infections is not recommended Additional information on efficacy in pediatric patients with infectious vancomycin-resistant Enterococcus faeciumLabelingB---Pfizer11/2/2005FALSE'
MESH:D00342412/5/2005zyvoxlinezolidCentral nervous system infectionsPK data in pediatric patients with ventriculoperitoneal shunts showed variable cerebrospinal fluid (CSF) concentrations; therapeutic concentrations were not consistently achieved or maintained in the CSF Use of linezolid for the empiric treatment of pediatric patients with central nervous system infections is not recommended Additional information on efficacy in pediatric patients with infectious vancomycin-resistant Enterococcus faeciumLabelingB---Pfizer11/2/2005FALSE'
MESH:D00342412/5/2005zyvoxlinezolidCentral nervous system infectionsPK data in pediatric patients with ventriculoperitoneal shunts showed variable cerebrospinal fluid (CSF) concentrations; therapeutic concentrations were not consistently achieved or maintained in the CSF Use of linezolid for the empiric treatment of pediatric patients with central nervous system infections is not recommended Additional information on efficacy in pediatric patients with infectious vancomycin-resistant Enterococcus faeciumLabelingB---Pfizer11/2/2005FALSE'
MESH:D00342403/25/2004ciprociprofloxacinComplicated UTI and pyelonephritisIndicated for the treatment of complicated urinary tract infections (cUTIs) and pyelonephritis in pediatric patients 1  17 years of age Not drug of first choice due to increased adverse events compared to controls including events related to joints and/or surrounding tissues Information on PK and dose in pediatric patients 1  17 years of age The most frequent adverse events observed within 6 weeks of treatment initiation during the cUTI clinical trial were gastrointestinal 15% compared to 9% and musculoskeletal 9.3% compared to 6% in ciprofloxacin-treated compared to control-treated patients, respectivelyLabelingB---Bayer12/18/2003FALSE'
MESH:D00342403/25/2004ciprociprofloxacinComplicated UTI and pyelonephritisIndicated for the treatment of complicated urinary tract infections (cUTIs) and pyelonephritis in pediatric patients 1  17 years of age Not drug of first choice due to increased adverse events compared to controls including events related to joints and/or surrounding tissues Information on PK and dose in pediatric patients 1  17 years of age The most frequent adverse events observed within 6 weeks of treatment initiation during the cUTI clinical trial were gastrointestinal 15% compared to 9% and musculoskeletal 9.3% compared to 6% in ciprofloxacin-treated compared to control-treated patients, respectivelyLabelingB---Bayer12/18/2003FALSE'
MESH:D0034242/11/2010ofirmevacetaminophenManagement of mild-to-moderate pain, for the management of moderate-to-severe pain with adjunctive opioid analgesics, and for the reduction of feverThe safety and effectiveness of Ofirmev for the treatment of acute pain and fever in pediatric patients ages 2 years and older is supported by evidence from adequate and well-controlled studies of Ofirmev in adults. Additional safety and PK data was collected in 355 from premature neonates to adolescents. The effectiveness of Ofirmev for the treatment of acute pain and fever has not been studied in pediatric patients < 2 years of age.The PK exposure of Ofirmev observed in children and adolescents is similar to adults, but higher in neonates and infants. Dosing simulations from PK data in infants and neonates suggest that dose reductions of 33% in infants 1 month to < 2 years of age, and 50% in neonates up to 28 days, with a minimum dosing interval of 6 hours, will produce a PK exposure similar to that observed in children age 2 years and olderMost common adverse reactions in pediatric patients were nausea, vomiting, constipation, pruritus, agitation, and atelectasis.Information on dosing, clinical studies, adverse reactions and PK parametersNew dosage form and route of administrationLabeling-P--Cadence-FALSE'
MESH:D00342401/27/2017ofirmevacetaminophenTreatmeny of pain and fever in pediatric patients birth to 2 yearsTreatment of pain Efficacy was not demonstrated in pediatric patients younger than 2 years in a double-blind, placebo-controlled study of 198 pediatric patients younger than 2 years. Pediatric patients less than 2 years of age, including neonates from 28 to 40 weeks gestational age at birth, were randomized to receive opioid plus acetaminophen or opioid plus placebo. No difference in analgesic effect of intravenous acetaminophen, measured by assessment of reduced need for additional opioid treatment for pain control, was observed. Treatment of fever The safety and effectiveness for the treatment of fever in pediatric patients, including premature neonates born at 32 weeks or greater gestation is supported by adequate and well-controlled studies of Ofirmev in adults, clinical studies in 244 pediatric patients 2 years and older, and safety and pharmacokinetic data from 239 patients younger than 2 years including neonates 32 weeks or greater gestational age. Information on dosing, clinical trials. Postmarketing study.Labeling--B,P-Mallinckrodt11/7/2016FALSE
MESH:D0034242/11/2010ofirmevacetaminophenManagement of mild-to-moderate pain, for the management of moderate-to-severe pain with adjunctive opioid analgesics, and for the reduction of feverThe safety and effectiveness of Ofirmev for the treatment of acute pain and fever in pediatric patients ages 2 years and older is supported by evidence from adequate and well-controlled studies of Ofirmev in adults. Additional safety and PK data was collected in 355 from premature neonates to adolescents. The effectiveness of Ofirmev for the treatment of acute pain and fever has not been studied in pediatric patients < 2 years of age.The PK exposure of Ofirmev observed in children and adolescents is similar to adults, but higher in neonates and infants. Dosing simulations from PK data in infants and neonates suggest that dose reductions of 33% in infants 1 month to < 2 years of age, and 50% in neonates up to 28 days, with a minimum dosing interval of 6 hours, will produce a PK exposure similar to that observed in children age 2 years and olderMost common adverse reactions in pediatric patients were nausea, vomiting, constipation, pruritus, agitation, and atelectasis.Information on dosing, clinical studies, adverse reactions and PK parametersNew dosage form and route of administrationLabeling-P--Cadence-FALSE'
MESH:D00342401/27/2017ofirmevacetaminophenTreatmeny of pain and fever in pediatric patients birth to 2 yearsTreatment of pain Efficacy was not demonstrated in pediatric patients younger than 2 years in a double-blind, placebo-controlled study of 198 pediatric patients younger than 2 years. Pediatric patients less than 2 years of age, including neonates from 28 to 40 weeks gestational age at birth, were randomized to receive opioid plus acetaminophen or opioid plus placebo. No difference in analgesic effect of intravenous acetaminophen, measured by assessment of reduced need for additional opioid treatment for pain control, was observed. Treatment of fever The safety and effectiveness for the treatment of fever in pediatric patients, including premature neonates born at 32 weeks or greater gestation is supported by adequate and well-controlled studies of Ofirmev in adults, clinical studies in 244 pediatric patients 2 years and older, and safety and pharmacokinetic data from 239 patients younger than 2 years including neonates 32 weeks or greater gestational age. Information on dosing, clinical trials. Postmarketing study.Labeling--B,P-Mallinckrodt11/7/2016FALSE