PedAM

Pediatric Disease Annotations & Medicines


	celiac disease

Disease ID	643
Disease	celiac disease
Definition	A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION.
Synonym	cd - celiac disease cd - coeliac disease celiac dis celiac disease (disorder) celiac disease [disease/finding] celiac disease nos celiac disease nos (disorder) celiac diseases celiac sprue celiac sprues celiac syndrome coeliac disease coeliac disease (disorder) coeliac disease [ambiguous] coeliac disease nos coeliac sprue coeliac syndrome cs - celiac sprue cs - coeliac sprue disease, celiac enteropathies, gluten enteropathies, gluten-sensitive enteropathy, gluten enteropathy, gluten-sensitive gluten enteropathies gluten enteropathy gluten intolerance gluten sensitive enteropathy gluten-induced enteropathy gluten-induced enteropathy syndrome gluten-responsive sprue gluten-sensitive enteropathies gluten-sensitive enteropathy gse - gluten-sensitive enteropathy idiopathic steatorrhea idiopathic steatorrhoea non tropical sprue non-tropical sprue nontropical sprue sprue sprue - nontropical sprue, celiac sprue, nontropical sprues steatorrhea - idiopathic steatorrhoea - idiopathic wheat-sensitive enteropathy
DOID	DOID:10608
ICD10	ICD10CM:K90.0
UMLS	C0007570
MeSH	D002446
SNOMED-CT	SNOMEDCT_US_2016_09_01:396331005
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:279) C0011854 \| type 1 diabetes \| 49 C0011847 \| diabetes \| 43 C0011854 \| type 1 diabetes mellitus \| 29 C0011849 \| diabetes mellitus \| 28 C0024299 \| lymphoma \| 18 C0021053 \| immune disease \| 16 C0011991 \| diarrhea \| 15 C0002871 \| anemia \| 13 C0024523 \| malabsorption \| 11 C0019158 \| hepatitis \| 10 C0022104 \| irritable bowel \| 10 C0007193 \| dilated cardiomyopathy \| 10 C0022104 \| irritable bowel syndrome \| 10 C0878544 \| cardiomyopathy \| 10 C0014544 \| epilepsy \| 7 C0021831 \| enteropathy \| 7 C0040128 \| thyroid disease \| 7 C0023895 \| liver disease \| 6 C0021831 \| bowel disease \| 6 C0029456 \| osteoporosis \| 6 C0020807 \| pulmonary hemosiderosis \| 5 C0162316 \| iron deficiency anemia \| 5 C0018799 \| heart disease \| 5 C0014868 \| esophagitis \| 5 C0021390 \| inflammatory bowel disease \| 5 C0948265 \| metabolic syndrome \| 5 C0001418 \| adenocarcinoma \| 5 C0011603 \| dermatitis \| 4 C0011570 \| depression \| 4 C0020676 \| hypothyroidism \| 4 C0021359 \| infertility \| 4 C0023890 \| cirrhosis \| 4 C0241910 \| autoimmune hepatitis \| 4 C0341106 \| eosinophilic esophagitis \| 4 C0149931 \| migraine \| 3 C0038363 \| aphthous stomatitis \| 3 C0007570 \| gluten intolerance \| 3 C0010346 \| crohn's disease \| 3 C0010674 \| cystic fibrosis \| 3 C0013473 \| eating disorders \| 3 C0028754 \| obesity \| 3 C0036341 \| schizophrenia \| 3 C0162429 \| malnutrition \| 3 C0041408 \| turner syndrome \| 3 C0920350 \| autoimmune thyroiditis \| 3 C0007570 \| sprue \| 3 C0002871 \| anaemia \| 3 C0042769 \| virus infection \| 3 C0013473 \| eating disorder \| 3 C0011608 \| dermatitis herpetiformis \| 3 C0019163 \| hepatitis b \| 3 C0162316 \| iron-deficiency anemia \| 3 C0007570 \| celiac disease \| 3 C0040053 \| thrombosis \| 3 C0019114 \| haemosiderosis \| 3 C0009319 \| colitis \| 2 C0005283 \| beta thalassemia \| 2 C0004134 \| ataxia \| 2 C0038362 \| stomatitis \| 2 C0027765 \| neurologic disorder \| 2 C0021053 \| immune disorders \| 2 C0400821 \| microscopic colitis \| 2 C0042870 \| vitamin d defic \| 2 C0019114 \| hemosiderosis \| 2 C0162316 \| iron deficiency anaemia \| 2 C0040188 \| tic disorders \| 2 C0020541 \| portal hypertension \| 2 C0040034 \| thrombocytopenia \| 2 C0033860 \| psoriasis \| 2 C0151744 \| ischaemic heart disease \| 2 C0020538 \| hypertension \| 2 C0022658 \| nephropathy \| 2 C0030305 \| pancreatitis \| 2 C0011854 \| diabetes mellitus type 1 \| 2 C0039730 \| thalassemia \| 2 C0026769 \| multiple sclerosis \| 2 C0019829 \| hodgkin lymphoma \| 2 C0023418 \| leukemia \| 2 C0022951 \| lactose intolerance \| 2 C0016470 \| food allergy \| 2 C0079731 \| b-cell lymphoma \| 2 C0162429 \| malnourished \| 2 C0042870 \| vitamin d deficiency \| 2 C0024523 \| intestinal malabsorption \| 2 C0002874 \| aplastic anemia \| 2 C0038238 \| steatorrhea \| 2 C0264793 \| idiopathic dilated cardiomyopathy \| 2 C0042109 \| urticaria \| 2 C0021053 \| immune disorder \| 2 C0040147 \| thyroiditis \| 2 C0017661 \| iga nephropathy \| 2 C0024523 \| malabsorption syndrome \| 2 C0011644 \| scleroderma \| 2 C0027765 \| neurologic disorders \| 2 C0041296 \| tuberculosis \| 2 C0029434 \| osteogenesis imperfecta \| 1 C0042373 \| vascular disease \| 1 C0011991 \| diarrhoea \| 1 C0270612 \| leukoencephalopathy \| 1 C0013295 \| duodenal ulceration \| 1 C0007137 \| squamous cell carcinoma \| 1 C0011616 \| contact dermatitis \| 1 C0011854 \| type i diabetes \| 1 C0031039 \| pericardial effusion \| 1 C0019196 \| hepatitis c \| 1 C0022408 \| arthropathy \| 1 C0018378 \| guillain barre syndrome \| 1 C0011351 \| enamel hypoplasia \| 1 C0342773 \| pearson syndrome \| 1 C0007222 \| cardiovascular disease \| 1 C0014547 \| partial epilepsy \| 1 C0020807 \| idiopathic pulmonary hemosiderosis \| 1 C0007115 \| thyroid cancer \| 1 C0031036 \| polyarteritis nodosa \| 1 C1140680 \| ovarian cancer \| 1 C0027765 \| neurological disorders \| 1 C0021843 \| intestinal obstruction \| 1 C0034212 \| pyoderma \| 1 C0027813 \| neuritis \| 1 C0037274 \| dermatosis \| 1 C0022661 \| chronic kidney disease \| 1 C0275911 \| intestinal tuberculosis \| 1 C0016053 \| fibromyalgia \| 1 C0267841 \| acalculous cholecystitis \| 1 C0003872 \| psoriatic arthritis \| 1 C0011854 \| insulin-dependent diabetes mellitus \| 1 C0011633 \| dermatomyositis \| 1 C0004943 \| behcet's disease \| 1 C0036202 \| sarcoidosis \| 1 C0020598 \| hypoglycemia \| 1 C0010068 \| coronary heart disease \| 1 C0011615 \| atopic dermatitis \| 1 C0023895 \| liver diseases \| 1 C0006370 \| bulimia \| 1 C0007789 \| cerebral palsy \| 1 C0085652 \| pyoderma gangrenosum \| 1 C0031069 \| familial mediterranean fever \| 1 C0008312 \| biliary cirrhosis \| 1 C0001973 \| alcoholism \| 1 C0281963 \| red cell aplasia \| 1 C0149931 \| migraine headache \| 1 C0566602 \| primary sclerosing cholangitis \| 1 C0022658 \| kidney disease \| 1 C0398623 \| hypercoagulability \| 1 C0001418 \| adenocarcinomas \| 1 C0003125 \| anorexia nervosa \| 1 C0026986 \| myelodysplastic syndromes \| 1 C0023473 \| chronic myeloid leukemia \| 1 C0025202 \| melanoma \| 1 C0042075 \| urological disorders \| 1 C0949272 \| ileocolitis \| 1 C0270922 \| demyelinating polyneuropathy \| 1 C0002170 \| alopecia \| 1 C0008313 \| sclerosing cholangitis \| 1 C1522378 \| large granular lymphocytic leukemia \| 1 C0242379 \| lung cancer \| 1 C0023530 \| leucopenia \| 1 C0023448 \| lymphocytic leukemia \| 1 C0856761 \| budd-chiari syndrome \| 1 C0023646 \| lichen planus \| 1 C0011334 \| caries \| 1 C0042109 \| urticarial \| 1 C0262587 \| parathyroid adenoma \| 1 C0021400 \| influenza \| 1 C0079774 \| peripheral t-cell lymphoma \| 1 C0013295 \| duodenal ulcer \| 1 C0011334 \| dental caries \| 1 C0162316 \| sideropenic anaemia \| 1 C0037315 \| sleep disordered breathing \| 1 C0020502 \| hyperparathyroidism \| 1 C0685938 \| gastrointestinal cancer \| 1 C0027873 \| neuromyelitis optica \| 1 C0034902 \| pure red cell aplasia \| 1 C0029442 \| osteomalacia \| 1 C0007130 \| mucinous adenocarcinoma \| 1 C0035258 \| restless legs syndrome \| 1 C0018213 \| grave's disease \| 1 C0267963 \| exocrine pancreatic insufficiency \| 1 C0024314 \| lymphoproliferative disorder \| 1 C0497327 \| dementia \| 1 C0018213 \| graves' disease \| 1 C0035258 \| restless legs syndrome (rls) \| 1 C0034152 \| henoch-schonlein purpura \| 1 C0025202 \| malignant melanoma \| 1 C0011854 \| insulin-dependent diabetes \| 1 C0017168 \| gastroesophageal reflux \| 1 C0004153 \| atherosclerosis \| 1 C0001197 \| acrodermatitis \| 1 C0014130 \| endocrine diseases \| 1 C0040128 \| thyroid disorders \| 1 C0685938 \| gi cancer \| 1 C0005586 \| bipolar disorder \| 1 C0024314 \| lymphoproliferative disorders \| 1 C0013395 \| dyspepsia \| 1 C0021933 \| intussusception \| 1 C0008311 \| cholangitis \| 1 C0002874 \| aplastic anaemia \| 1 C0042164 \| uveitis \| 1 C0016053 \| fibromyalgia syndrome \| 1 C0021390 \| inflammatory bowel diseases \| 1 C0221036 \| acrodermatitis enteropathica \| 1 C0398623 \| thrombophilia \| 1 C0022658 \| renal disease \| 1 C0019202 \| wilson's disease \| 1 C0002886 \| macrocytic anemia \| 1 C0028326 \| noonan syndrome \| 1 C0009806 \| constipation \| 1 C0018801 \| heart failure \| 1 C0085278 \| antiphospholipid syndrome \| 1 C0398791 \| nijmegen breakage syndrome \| 1 C0017168 \| esophageal reflux \| 1 C0036421 \| systemic sclerosis \| 1 C0017168 \| oesophageal reflux \| 1 C0242490 \| enthesopathy \| 1 C0007115 \| thyroid ca \| 1 C0007102 \| colon cancer \| 1 C0151779 \| cutaneous malignant melanoma \| 1 C0015230 \| rash \| 1 C0027121 \| myositis \| 1 C0035258 \| restless legs \| 1 C0016412 \| folate deficiency \| 1 C0149922 \| lichen simplex chronicus \| 1 C1140680 \| ovarian ca \| 1 C0037280 \| infestation \| 1 C0001430 \| adenoma \| 1 C0152025 \| polyneuropathy \| 1 C1302401 \| colorectal adenoma \| 1 C0027059 \| myocarditis \| 1 C0035579 \| rickets \| 1 C0023895 \| diseases of the liver \| 1 C0026848 \| myopathy \| 1 C0037274 \| skin disease \| 1 C0600260 \| obstructive pulmonary disease \| 1 C0020676 \| hypothyroid \| 1 C1527336 \| sjogren's syndrome \| 1 C0162429 \| nutritional deficiencies \| 1 C0836924 \| thrombocytosis \| 1 C0002171 \| alopecia areata \| 1 C0034150 \| purpura \| 1 C0020807 \| idiopathic pulmonary haemosiderosis \| 1 C0022661 \| end-stage renal disease \| 1 C0025958 \| microcephaly \| 1 C0175702 \| williams-beuren syndrome \| 1 C0003864 \| arthritis \| 1 C1510471 \| vitamin deficiencies \| 1 C0009763 \| conjunctivitis \| 1 C0023470 \| myeloid leukemia \| 1 C0026986 \| myelodysplastic syndrome \| 1 C0024305 \| non-hodgkin lymphoma \| 1 C0015974 \| periodic fever \| 1 C0005940 \| bone disease \| 1 C0032266 \| pneumatosis cystoides intestinalis \| 1 C0151468 \| thyroid adenoma \| 1 C0235974 \| pancreatic carcinoma \| 1 C0598608 \| hyperhomocysteinemia \| 1 C0024117 \| chronic obstructive pulmonary disease \| 1 C0151544 \| gastrointestinal carcinoma \| 1 C0023798 \| lipomas \| 1 C0014130 \| endocrine disease \| 1 C0279626 \| squamous cell carcinoma of the esophagus \| 1 C0017154 \| atrophic gastritis \| 1 C0001339 \| acute pancreatitis \| 1 C0036416 \| scleritis \| 1 C0027765 \| neurological disorder \| 1 C0085669 \| acute leukemia \| 1 C0004352 \| autism \| 1 C0017152 \| gastritis \| 1 C0002736 \| amyotrophic lateral sclerosis \| 1 C0392525 \| nephrolithiasis \| 1 C0024115 \| pulmonary disease \| 1 C0029134 \| optic neuritis \| 1 C0007758 \| cerebellar ataxia \| 1 C0007570 \| gluten-sensitive enteropathy \| 1 C0030293 \| pancreatic insufficiency \| 1 C0021845 \| intestinal perforation \| 1 C0007570 \| coeliac disease \| 1 C0014175 \| endometriosis \| 1 C1522378 \| large granular lymphocytosis \| 1 C0010308 \| congenital hypothyroidism \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:44) HLA-DQA1 \| 3117 \| CTD_human;GWASCAT;GHR BACH2 \| 60468 \| CTD_human;GWASCAT CTLA4 \| 1493 \| CTD_human RUNX3 \| 864 \| CTD_human NKAIN2 \| 154215 \| GWASCAT ATXN2 \| 6311 \| GWASCAT HLA-DPB1 \| 3115 \| CTD_human KIAA1109 \| 84162 \| GWASCAT IL21 \| 59067 \| CTD_human HLA-DQB1 \| 3119 \| CTD_human;GHR ACACA \| 31 \| GWASCAT ICOS \| 29851 \| GWASCAT WNT3 \| 7473 \| GWASCAT NFIA \| 4774 \| GWASCAT TGM2 \| 7052 \| CTD_human THEMIS \| 387357 \| CTD_human CD80 \| 941 \| CTD_human ELMO1 \| 9844 \| GWASCAT CD247 \| 919 \| GWASCAT IL12A-AS1 \| 101928376 \| GWASCAT TAGAP \| 117289 \| GWASCAT PTPN2 \| 5771 \| GWASCAT IL15 \| 3600 \| CTD_human CCR4 \| 1233 \| CTD_human ETS1 \| 2113 \| CTD_human;GWASCAT CELIAC2 \| 317782 \| CTD_human SH2B3 \| 10019 \| CTD_human PUS10 \| 150962 \| GWASCAT MYO9B \| 4650 \| CTD_human ZMIZ1 \| 57178 \| CTD_human;GWASCAT FRMD4B \| 23150 \| GWASCAT PLEK \| 5341 \| GWASCAT ICOSLG \| 23308 \| CTD_human;GWASCAT MYNN \| 55892 \| GWASCAT TNFRSF14 \| 8764 \| CTD_human DLEU1 \| 10301 \| GWASCAT UQCRC2P1 \| 100131327 \| GWASCAT ARHGAP31 \| 57514 \| GWASCAT LPP \| 4026 \| GWASCAT MMEL1 \| 79258 \| GWASCAT IL18R1 \| 8809 \| GWASCAT PPP1R12B \| 4660 \| GWASCAT YDJC \| 150223 \| GWASCAT C17orf78 \| 284099 \| GWASCAT
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:156) 132612 \| ADAD1 \| infer 130872 \| AHSA2 \| infer 57514 \| ARHGAP31 \| infer 6311 \| ATXN2 \| infer 60468 \| BACH2 \| infer 6347 \| CCL2 \| infer 6352 \| CCL5 \| infer 1230 \| CCR1 \| infer 729230 \| CCR2 \| infer 1232 \| CCR3 \| infer 1233 \| CCR4 \| infer 1234 \| CCR5 \| infer 10803 \| CCR9 \| infer 9034 \| CCRL2 \| infer 929 \| CD14 \| infer 30835 \| CD209 \| infer 919 \| CD247 \| infer 940 \| CD28 \| infer 915 \| CD3D \| infer 916 \| CD3E \| infer 917 \| CD3G \| infer 972 \| CD74 \| infer 941 \| CD80 \| infer 942 \| CD86 \| infer 4261 \| CIITA \| infer 23274 \| CLEC16A \| infer 1493 \| CTLA4 \| infer 414325 \| DEFB103A \| infer 140596 \| DEFB104A \| infer 1760 \| DMPK \| infer 56940 \| DUSP22 \| infer 9844 \| ELMO1 \| infer 2113 \| ETS1 \| infer 355 \| FAS \| infer 356 \| FASLG \| infer 2246 \| FGF1 \| infer 50943 \| FOXP3 \| infer 23150 \| FRMD4B \| infer 3105 \| HLA-A \| infer 3106 \| HLA-B \| infer 3107 \| HLA-C \| infer 3115 \| HLA-DPB1 \| infer 3117 \| HLA-DQA1 \| infer 3119 \| HLA-DQB1 \| infer 3122 \| HLA-DRA \| infer 3123 \| HLA-DRB1 \| infer 3127 \| HLA-DRB5 \| infer 3135 \| HLA-G \| infer 3240 \| HP \| infer 3383 \| ICAM1 \| infer 29851 \| ICOS \| infer 23308 \| ICOSLG \| infer 3458 \| IFNG \| infer 3550 \| IK \| infer 3586 \| IL10 \| infer 3587 \| IL10RA \| infer 3592 \| IL12A \| infer 3593 \| IL12B \| infer 3596 \| IL13 \| infer 27190 \| IL17B \| infer 3606 \| IL18 \| infer 8809 \| IL18R1 \| infer 8807 \| IL18RAP \| infer 3552 \| IL1A \| infer 3553 \| IL1B \| infer 9173 \| IL1RL1 \| infer 8808 \| IL1RL2 \| infer 3557 \| IL1RN \| infer 3558 \| IL2 \| infer 59067 \| IL21 \| infer 3562 \| IL3 \| infer 3565 \| IL4 \| infer 3567 \| IL5 \| infer 3569 \| IL6 \| infer 3570 \| IL6R \| infer 3578 \| IL9 \| infer 3659 \| IRF1 \| infer 3662 \| IRF4 \| infer 3676 \| ITGA4 \| infer 9832 \| JAKMIP2 \| infer 84162 \| KIAA1109 \| infer 3802 \| KIR2DL1 \| infer 3803 \| KIR2DL2 \| infer 3804 \| KIR2DL3 \| infer 57292 \| KIR2DL5A \| infer 553128 \| KIR2DL5B \| infer 11026 \| LILRA3 \| infer 4026 \| LPP \| infer 4049 \| LTA \| infer 6885 \| MAP3K7 \| infer 4153 \| MBL2 \| infer 100507436 \| MICA \| infer 4277 \| MICB \| infer 79258 \| MMEL1 \| infer 4312 \| MMP1 \| infer 4314 \| MMP3 \| infer 359758 \| MRPS17P5 \| infer 4524 \| MTHFR \| infer 55892 \| MYNN \| infer 4650 \| MYO9B \| infer 4774 \| NFIA \| infer 4790 \| NFKB1 \| infer 64127 \| NOD2 \| infer 2908 \| NR3C1 \| infer 167826 \| OLIG3 \| infer 11315 \| PARK7 \| infer 5341 \| PLEK \| infer 5619 \| PRM1 \| infer 5771 \| PTPN2 \| infer 26191 \| PTPN22 \| infer 5796 \| PTPRK \| infer 150962 \| PUS10 \| infer 5820 \| PVT1 \| infer 5966 \| REL \| infer 5996 \| RGS1 \| infer 431704 \| RGS21 \| infer 100270859 \| RPS2P19 \| infer 864 \| RUNX3 \| infer 29970 \| SCHIP1 \| infer 6401 \| SELE \| infer 6402 \| SELL \| infer 10019 \| SH2B3 \| infer 153201 \| SLC36A2 \| infer 389015 \| SLC9A4 \| infer 8651 \| SOCS1 \| infer 6690 \| SPINK1 \| infer 6691 \| SPINK2 \| infer 27290 \| SPINK4 \| infer 11005 \| SPINK5 \| infer 145165 \| ST13P4 \| infer 202374 \| STK32A \| infer 117289 \| TAGAP \| infer 10915 \| TCERG1 \| infer 7040 \| TGFB1 \| infer 7042 \| TGFB2 \| infer 7052 \| TGM2 \| infer 387357 \| THEMIS \| infer 7070 \| THY1 \| infer 25976 \| TIPARP \| infer 7099 \| TLR4 \| infer 51284 \| TLR7 \| infer 51311 \| TLR8 \| infer 7124 \| TNF \| infer 7128 \| TNFAIP3 \| infer 8764 \| TNFRSF14 \| infer 3604 \| TNFRSF9 \| infer 8995 \| TNFSF18 \| infer 7292 \| TNFSF4 \| infer 10477 \| UBE2E3 \| infer 7332 \| UBE2L3 \| infer 7473 \| WNT3 \| infer 2829 \| XCR1 \| infer 150223 \| YDJC \| infer 81555 \| YIPF5 \| infer 677 \| ZFP36L1 \| infer 57178 \| ZMIZ1 \| infer
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:334) 100506492 \| DSCAM-AS1 \| DISEASES 920 \| CD4 \| DISEASES 64132 \| XYLT2 \| DISEASES 6343 \| SCT \| DISEASES 30009 \| TBX21 \| DISEASES 343641 \| TGM6 \| DISEASES 266 \| AMELY \| DISEASES 3956 \| LGALS1 \| DISEASES 3560 \| IL2RB \| DISEASES 3002 \| GZMB \| DISEASES 479 \| ATP12A \| DISEASES 50855 \| PARD6A \| DISEASES 7038 \| TG \| DISEASES 83988 \| NCALD \| DISEASES 8797 \| TNFRSF10A \| DISEASES 4051 \| CYP4F3 \| DISEASES 8529 \| CYP4F2 \| DISEASES 973 \| CD79A \| DISEASES 7461 \| CLIP2 \| DISEASES 4353 \| MPO \| DISEASES 6143 \| RPL19 \| DISEASES 5539 \| PPY \| DISEASES 51056 \| LAP3 \| DISEASES 3558 \| IL2 \| DISEASES 56253 \| CRTAM \| DISEASES 969 \| CD69 \| DISEASES 2735 \| GLI1 \| DISEASES 3458 \| IFNG \| DISEASES 3820 \| KLRB1 \| DISEASES 10279 \| PRSS16 \| DISEASES 2690 \| GHR \| DISEASES 3565 \| IL4 \| DISEASES 3567 \| IL5 \| DISEASES 8440 \| NCK2 \| DISEASES 8809 \| IL18R1 \| DISEASES 116444 \| GRIN3B \| DISEASES 6402 \| SELL \| DISEASES 7128 \| TNFAIP3 \| DISEASES 5507 \| PPP1R3C \| DISEASES 22914 \| KLRK1 \| DISEASES 3581 \| IL9R \| DISEASES 2806 \| GOT2 \| DISEASES 3659 \| IRF1 \| DISEASES 1446 \| CSN1S1 \| DISEASES 968 \| CD68 \| DISEASES 3630 \| INS \| DISEASES 7283 \| TUBG1 \| DISEASES 8220 \| DGCR14 \| DISEASES 4277 \| MICB \| DISEASES 3000 \| GUCY2D \| DISEASES 1401 \| CRP \| DISEASES 23743 \| BHMT2 \| DISEASES 4922 \| NTS \| DISEASES 9398 \| CD101 \| DISEASES 2694 \| GIF \| DISEASES 60468 \| BACH2 \| DISEASES 6302 \| TSPAN31 \| DISEASES 3569 \| IL6 \| DISEASES 2572 \| GAD2 \| DISEASES 27348 \| TOR1B \| DISEASES 7097 \| TLR2 \| DISEASES 8836 \| GGH \| DISEASES 84888 \| SPPL2A \| DISEASES 3595 \| IL12RB2 \| DISEASES 10847 \| SRCAP \| DISEASES 495 \| ATP4A \| DISEASES 57644 \| MYH7B \| DISEASES 27134 \| TJP3 \| DISEASES 3682 \| ITGAE \| DISEASES 1 \| A1BG \| DISEASES 5588 \| PRKCQ \| DISEASES 3552 \| IL1A \| DISEASES 3553 \| IL1B \| DISEASES 55717 \| WDR11 \| DISEASES 943 \| TNFRSF8 \| DISEASES 905 \| CCNT2 \| DISEASES 23518 \| R3HDM1 \| DISEASES 3938 \| LCT \| DISEASES 832 \| CAPZB \| DISEASES 941 \| CD80 \| DISEASES 8807 \| IL18RAP \| DISEASES 6476 \| SI \| DISEASES 59067 \| IL21 \| DISEASES 84162 \| KIAA1109 \| DISEASES 3383 \| ICAM1 \| DISEASES 5523 \| PPP2R3A \| DISEASES 23242 \| COBL \| DISEASES 6523 \| SLC5A1 \| DISEASES 3687 \| ITGAX \| DISEASES 402665 \| IGLON5 \| DISEASES 2169 \| FABP2 \| DISEASES 3001 \| GZMA \| DISEASES 3578 \| IL9 \| DISEASES 8795 \| TNFRSF10B \| DISEASES 4715 \| NDUFB9 \| DISEASES 3439 \| IFNA1 \| DISEASES 51144 \| HSD17B12 \| DISEASES 2206 \| MS4A2 \| DISEASES 10666 \| CD226 \| DISEASES 3606 \| IL18 \| DISEASES 9472 \| AKAP6 \| DISEASES 7082 \| TJP1 \| DISEASES 115106 \| HAUS1 \| DISEASES 5741 \| PTH \| DISEASES 5651 \| TMPRSS15 \| DISEASES 4645 \| MYO5B \| DISEASES 9073 \| CLDN8 \| DISEASES 6750 \| SST \| DISEASES 26060 \| APPL1 \| DISEASES 539 \| ATP5O \| DISEASES 326 \| AIRE \| DISEASES 9437 \| NCR1 \| DISEASES 162417 \| NAGS \| DISEASES 1990 \| CELA1 \| DISEASES 2215 \| FCGR3B \| DISEASES 5966 \| REL \| DISEASES 389015 \| SLC9A4 \| DISEASES 5798 \| PTPRN \| DISEASES 213 \| ALB \| DISEASES 132014 \| IL17RE \| DISEASES 54859 \| ELP6 \| DISEASES 4085 \| MAD2L1 \| DISEASES 132612 \| ADAD1 \| DISEASES 3600 \| IL15 \| DISEASES 7098 \| TLR3 \| DISEASES 4982 \| TNFRSF11B \| DISEASES 1672 \| DEFB1 \| DISEASES 115825 \| WDFY2 \| DISEASES 4314 \| MMP3 \| DISEASES 290 \| ANPEP \| DISEASES 25895 \| METTL21B \| DISEASES 64127 \| NOD2 \| DISEASES 94235 \| GNG8 \| DISEASES 3906 \| LALBA \| DISEASES 5617 \| PRL \| DISEASES 6037 \| RNASE3 \| DISEASES 3479 \| IGF1 \| DISEASES 3308 \| HSPA4 \| DISEASES 3592 \| IL12A \| DISEASES 1493 \| CTLA4 \| DISEASES 5068 \| REG3A \| DISEASES 3575 \| IL7R \| DISEASES 84684 \| INSM2 \| DISEASES 56246 \| MRAP \| DISEASES 654483 \| BOLA2B \| DISEASES 27087 \| B3GAT1 \| DISEASES 79660 \| PPP1R3B \| DISEASES 2147 \| F2 \| DISEASES 24146 \| CLDN15 \| DISEASES 1521 \| CTSW \| DISEASES 5771 \| PTPN2 \| DISEASES 924 \| CD7 \| DISEASES 9844 \| ELMO1 \| DISEASES 3952 \| LEP \| DISEASES 258 \| AMBN \| DISEASES 10102 \| TSFM \| DISEASES 2907 \| GRINA \| DISEASES 4261 \| CIITA \| DISEASES 4026 \| LPP \| DISEASES 4684 \| NCAM1 \| DISEASES 7173 \| TPO \| DISEASES 140596 \| DEFB104A \| DISEASES 811 \| CALR \| DISEASES 149233 \| IL23R \| DISEASES 503618 \| DEFB104B \| DISEASES 51066 \| SSUH2 \| DISEASES 63925 \| ZNF335 \| DISEASES 150962 \| PUS10 \| DISEASES 23046 \| KIF21B \| DISEASES 8651 \| SOCS1 \| DISEASES 1850 \| DUSP8 \| DISEASES 1670 \| DEFA5 \| DISEASES 83479 \| DDX59 \| DISEASES 552900 \| BOLA2 \| DISEASES 2520 \| GAST \| DISEASES 942 \| CD86 \| DISEASES 682 \| BSG \| DISEASES 57178 \| ZMIZ1 \| DISEASES 164656 \| TMPRSS6 \| DISEASES 51738 \| GHRL \| DISEASES 885 \| CCK \| DISEASES 5569 \| PKIA \| DISEASES 9075 \| CLDN2 \| DISEASES 677 \| ZFP36L1 \| DISEASES 112744 \| IL17F \| DISEASES 3363 \| HTR7 \| DISEASES 3824 \| KLRD1 \| DISEASES 23436 \| CELA3B \| DISEASES 114904 \| C1QTNF6 \| DISEASES 3117 \| HLA-DQA1 \| DISEASES 85480 \| TSLP \| DISEASES 3329 \| HSPD1 \| DISEASES 79722 \| ANKRD55 \| DISEASES 1364 \| CLDN4 \| DISEASES 921 \| CD5 \| DISEASES 159296 \| NKX2-3 \| DISEASES 3605 \| IL17A \| DISEASES 7332 \| UBE2L3 \| DISEASES 10019 \| SH2B3 \| DISEASES 1861 \| TOR1A \| DISEASES 9863 \| MAGI2 \| DISEASES 100506658 \| OCLN \| DISEASES 5265 \| SERPINA1 \| DISEASES 3240 \| HP \| DISEASES 51256 \| TBC1D7 \| DISEASES 130872 \| AHSA2 \| DISEASES 987 \| LRBA \| DISEASES 2695 \| GIP \| DISEASES 10803 \| CCR9 \| DISEASES 1121 \| CHM \| DISEASES 3821 \| KLRC1 \| DISEASES 26191 \| PTPN22 \| DISEASES 3123 \| HLA-DRB1 \| DISEASES 5697 \| PYY \| DISEASES 7037 \| TFRC \| DISEASES 3135 \| HLA-G \| DISEASES 1803 \| DPP4 \| DISEASES 5646 \| PRSS3 \| DISEASES 916 \| CD3E \| DISEASES 7052 \| TGM2 \| DISEASES 55532 \| SLC30A10 \| DISEASES 117289 \| TAGAP \| DISEASES 9580 \| SOX13 \| DISEASES 55765 \| C1orf106 \| DISEASES 353091 \| RAET1G \| DISEASES 5788 \| PTPRC \| DISEASES 5996 \| RGS1 \| DISEASES 356 \| FASLG \| DISEASES 167826 \| OLIG3 \| DISEASES 2214 \| FCGR3A \| DISEASES 5796 \| PTPRK \| DISEASES 632 \| BGLAP \| DISEASES 7062 \| TCHH \| DISEASES 5550 \| PREP \| DISEASES 914 \| CD2 \| DISEASES 8269 \| TMEM187 \| DISEASES 22854 \| NTNG1 \| DISEASES 158511 \| CSAG1 \| DISEASES 959 \| CD40LG \| DISEASES 9436 \| NCR2 \| DISEASES 5090 \| PBX3 \| DISEASES 200081 \| TXLNA \| DISEASES 7099 \| TLR4 \| DISEASES 1043 \| CD52 \| DISEASES 56288 \| PARD3 \| DISEASES 3108 \| HLA-DMA \| DISEASES 229 \| ALDOB \| DISEASES 3118 \| HLA-DQA2 \| DISEASES 7918 \| GPANK1 \| DISEASES 57827 \| C6orf47 \| DISEASES 50943 \| FOXP3 \| DISEASES 100507436 \| MICA \| DISEASES 3107 \| HLA-C \| DISEASES 1041 \| CDSN \| DISEASES 4524 \| MTHFR \| DISEASES 3133 \| HLA-E \| DISEASES 3105 \| HLA-A \| DISEASES 23130 \| ATG2A \| DISEASES 6311 \| ATXN2 \| DISEASES 8718 \| TNFRSF25 \| DISEASES 57623 \| ZFAT \| DISEASES 441376 \| AARD \| DISEASES 79258 \| MMEL1 \| DISEASES 9308 \| CD83 \| DISEASES 3096 \| HIVEP1 \| DISEASES 10186 \| LHFP \| DISEASES 27290 \| SPINK4 \| DISEASES 5209 \| PFKFB3 \| DISEASES 3559 \| IL2RA \| DISEASES 54790 \| TET2 \| DISEASES 265 \| AMELX \| DISEASES 3486 \| IGFBP3 \| DISEASES 2813 \| GP2 \| DISEASES 7053 \| TGM3 \| DISEASES 3822 \| KLRC2 \| DISEASES 3823 \| KLRC3 \| DISEASES 6370 \| CCL25 \| DISEASES 147700 \| KLC3 \| DISEASES 3898 \| LAD1 \| DISEASES 55054 \| ATG16L1 \| DISEASES 65057 \| ACD \| DISEASES 91807 \| MYLK3 \| DISEASES 4891 \| SLC11A2 \| DISEASES 1365 \| CLDN3 \| DISEASES 81606 \| LBH \| DISEASES 2958 \| GTF2A2 \| DISEASES 4650 \| MYO9B \| DISEASES 23150 \| FRMD4B \| DISEASES 3119 \| HLA-DQB1 \| DISEASES 3803 \| KIR2DL2 \| DISEASES 23308 \| ICOSLG \| DISEASES 4660 \| PPP1R12B \| DISEASES 91319 \| DERL3 \| DISEASES 8995 \| TNFSF18 \| DISEASES 3238 \| HOXD12 \| DISEASES 7018 \| TF \| DISEASES 23274 \| CLEC16A \| DISEASES 4295 \| MLN \| DISEASES 3120 \| HLA-DQB2 \| DISEASES 5537 \| PPP6C \| DISEASES 720 \| C4A \| DISEASES 10107 \| TRIM10 \| DISEASES 960 \| CD44 \| DISEASES 7124 \| TNF \| DISEASES 3106 \| HLA-B \| DISEASES 25989 \| ULK3 \| DISEASES 7072 \| TIA1 \| DISEASES 339804 \| C2orf74 \| DISEASES 3594 \| IL12RB1 \| DISEASES 29970 \| SCHIP1 \| DISEASES 84671 \| ZNF347 \| DISEASES 3115 \| HLA-DPB1 \| DISEASES 34 \| ACADM \| DISEASES 3586 \| IL10 \| DISEASES 5527 \| PPP2R5C \| DISEASES 169026 \| SLC30A8 \| DISEASES 721 \| C4B \| DISEASES 143662 \| MUC15 \| DISEASES 3077 \| HFE \| DISEASES 65980 \| BRD9 \| DISEASES 51428 \| DDX41 \| DISEASES 431704 \| RGS21 \| DISEASES 917 \| CD3G \| DISEASES 9414 \| TJP2 \| DISEASES 387357 \| THEMIS \| DISEASES 10603 \| SH2B2 \| DISEASES 1232 \| CCR3 \| DISEASES 10198 \| MPHOSPH9 \| DISEASES 567 \| B2M \| DISEASES 64772 \| ENGASE \| DISEASES 10866 \| HCP5 \| DISEASES 348120 \| LINC01193 \| DISEASES 677768 \| SCARNA13 \| DISEASES 26796 \| SNORD53 \| DISEASES
Locus	(Waiting for update.)

Disease ID	643
Disease	celiac disease
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:172) HP:0000819 \| Diabetes mellitus \| 28 HP:0002960 \| Autoimmune condition \| 25 HP:0011473 \| Villous atrophy \| 24 HP:0002665 \| Lymphoma \| 17 HP:0001903 \| Anemia \| 16 HP:0002014 \| Diarrhea \| 15 HP:0002024 \| Intestinal malabsorption \| 12 HP:0001644 \| Congestive cardiomyopathy \| 10 HP:0012115 \| Liver inflammation \| 10 HP:0001638 \| Cardiomyopathy \| 10 HP:0001891 \| Iron-deficiency anemia \| 8 HP:0012190 \| T cell lymphoma \| 8 HP:0002242 \| Enteropathy \| 7 HP:0000820 \| Thyroid abnormality \| 7 HP:0012531 \| Pain \| 7 HP:0012538 \| Gluten sensitivity \| 6 HP:0000939 \| Osteoporosis \| 6 HP:0002027 \| Abdominal pain \| 5 HP:0100633 \| Inflammation of the esophagus \| 5 HP:0002028 \| Chronic diarrhea \| 5 HP:0001824 \| Weight loss \| 4 HP:0000821 \| Underactive thyroid \| 4 HP:0001397 \| Hepatic steatosis \| 4 HP:0000716 \| Depression \| 4 HP:0001394 \| Hepatic cirrhosis \| 4 HP:0000789 \| Infertility \| 4 HP:0100280 \| Morbus Crohn \| 3 HP:0100753 \| Schizophrenia \| 3 HP:0002664 \| Neoplasia \| 3 HP:0002608 \| Celiac disease \| 3 HP:0004322 \| Stature below 3rd percentile \| 3 HP:0004395 \| Malnutrition \| 3 HP:0030731 \| Carcinoma \| 3 HP:0001513 \| Obesity \| 3 HP:0002076 \| Migraine headaches \| 3 HP:0002720 \| Decreased immunoglobulin A \| 3 HP:0002239 \| Gastrointestinal hemorrhage \| 2 HP:0001733 \| Pancreatic inflammation \| 2 HP:0010783 \| Erythema \| 2 HP:0002570 \| Steatorrhea \| 2 HP:0002584 \| Intestinal hemorrhage \| 2 HP:0100724 \| Hypercoagulability \| 2 HP:0011107 \| Recurrent aphthous stomatitis \| 2 HP:0011458 \| Abdominal symptom \| 2 HP:0012414 \| Duodenal atrophy \| 2 HP:0000112 \| Nephropathy \| 2 HP:0012191 \| B-cell lymphoma \| 2 HP:0100646 \| Thyroiditis \| 2 HP:0001909 \| Leukemia \| 2 HP:0100033 \| Tic disorder \| 2 HP:0002315 \| Headaches \| 2 HP:0002583 \| Colitis \| 2 HP:0200123 \| Chronic liver inflammation \| 2 HP:0004789 \| Lactose intolerance \| 2 HP:0003765 \| Psoriasis \| 2 HP:0001873 \| Low platelet count \| 2 HP:0001915 \| Aplastic anemia \| 2 HP:0100324 \| Progressive systemic scleroderma \| 2 HP:0002910 \| Elevated transaminases \| 2 HP:0100827 \| Lymphocytosis \| 2 HP:0005110 \| Atrial fibrillation \| 2 HP:0001025 \| Hives \| 2 HP:0001409 \| Portal hypertension \| 2 HP:0001880 \| Eosinophilia \| 2 HP:0012189 \| Hodgkin disease \| 2 HP:0100512 \| Vitamin D deficiency \| 2 HP:0001251 \| Ataxia \| 2 HP:0000822 \| Hypertension \| 2 HP:0012450 \| Chronic constipation \| 1 HP:0000252 \| Small head circumference \| 1 HP:0000854 \| Thyroid adenoma \| 1 HP:0000726 \| Dementia \| 1 HP:0001263 \| Developmental retardation \| 1 HP:0003270 \| Distended abdomen \| 1 HP:0012219 \| Erythema nodosum \| 1 HP:0006510 \| Chronic obstructive pulmonary disease \| 1 HP:0001698 \| Pericardial effusions \| 1 HP:0004386 \| Gastrointestinal inflammation \| 1 HP:0005263 \| Gastritis \| 1 HP:0012393 \| Allergy \| 1 HP:0002639 \| Budd-Chiari syndrome \| 1 HP:0000843 \| Hyperparathyroidism \| 1 HP:0001972 \| Macrocytic anemia \| 1 HP:0030151 \| Cholangitis \| 1 HP:0005506 \| Chronic myeloid leukemia \| 1 HP:0002653 \| Bone pain \| 1 HP:0000509 \| Conjunctivitis \| 1 HP:0001508 \| Weight faltering \| 1 HP:0000708 \| Behavioral problems \| 1 HP:0001047 \| Atopic dermatitis \| 1 HP:0007354 \| Amyotrophic lateral sclerosis \| 1 HP:0000851 \| Congenital hypothyroidism \| 1 HP:0001012 \| Multiple lipomas \| 1 HP:0002613 \| Biliary cirrhosis \| 1 HP:0100653 \| Optic neuritis \| 1 HP:0002748 \| Rickets \| 1 HP:0010280 \| Stomatitis \| 1 HP:0002488 \| Acute leukemias \| 1 HP:0002901 \| Hypocalcemia \| 1 HP:0100532 \| Scleritis \| 1 HP:0012378 \| Fatigue \| 1 HP:0000979 \| Purpura \| 1 HP:0012452 \| Restless legs \| 1 HP:0003774 \| End-stage renal failure \| 1 HP:0001548 \| Overgrowth \| 1 HP:0002273 \| Tetraparesis \| 1 HP:0006297 \| Hypoplasia of tooth enamel \| 1 HP:0002019 \| Dyschezia \| 1 HP:0001894 \| Thrombocytosis \| 1 HP:0000670 \| Dental caries \| 1 HP:0002672 \| Gastrointestinal carcinoma \| 1 HP:0002352 \| Leukoencephalopathy \| 1 HP:0002625 \| Blood clot in a deep vein \| 1 HP:0000554 \| Uveitis \| 1 HP:0002251 \| Hirschsprung megacolon \| 1 HP:0002861 \| Melanoma \| 1 HP:0002749 \| Osteomalacia \| 1 HP:0005202 \| Helicobacter pylori infection \| 1 HP:0001518 \| Small for gestational age \| 1 HP:0000787 \| Renal calculi \| 1 HP:0001271 \| Polyneuropathy \| 1 HP:0012324 \| Myeloid leukemia \| 1 HP:0003198 \| Myopathic changes \| 1 HP:0003470 \| Inability to move \| 1 HP:0005523 \| Lymphoproliferative disorder \| 1 HP:0002020 \| Heartburn \| 1 HP:0001919 \| Acute renal failure \| 1 HP:0002576 \| Intussusception \| 1 HP:0001635 \| Congestive heart failure \| 1 HP:0003040 \| Arthropathy \| 1 HP:0001943 \| Hypoglycemia \| 1 HP:0001596 \| Hair loss \| 1 HP:0002105 \| Hemoptysis \| 1 HP:0001735 \| Acute pancreatitis \| 1 HP:0002588 \| Duodenal ulcer \| 1 HP:0007302 \| Bipolar disorder \| 1 HP:0006980 \| Progressive leukoencephalopathy \| 1 HP:0002719 \| infections, recurrent \| 1 HP:0100507 \| Folate deficiency \| 1 HP:0000684 \| Delayed eruption of teeth \| 1 HP:0000144 \| Decreased fertility \| 1 HP:0100021 \| Cerebral palsy \| 1 HP:0001627 \| Congenital heart defects \| 1 HP:0012622 \| Chronic kidney disease \| 1 HP:0000938 \| Decreased bone mineral density \| 1 HP:0001324 \| Muscular weakness \| 1 HP:0001285 \| Spastic tetraparesis \| 1 HP:0002863 \| Myelodysplastic syndrome \| 1 HP:0003003 \| Colon cancer \| 1 HP:0012410 \| Pure red cell aplasia \| 1 HP:0001738 \| Exocrine pancreatic insufficiency \| 1 HP:0002072 \| Chorea \| 1 HP:0005214 \| Bowel obstruction \| 1 HP:0002039 \| Anorexia \| 1 HP:0000999 \| Pyoderma \| 1 HP:0100739 \| Binge and purge \| 1 HP:0100543 \| Cognitive deficits \| 1 HP:0012539 \| Non-Hodgkin lymphoma \| 1 HP:0002229 \| Alopecia areata \| 1 HP:0002897 \| Parathyroid adenoma \| 1 HP:0001297 \| Cerebral vascular events \| 1 HP:0001993 \| Ketoacidosis \| 1 HP:0100614 \| Muscle inflammation \| 1 HP:0001369 \| Arthritis \| 1 HP:0001945 \| Fever \| 1 HP:0030127 \| Endometriosis \| 1 HP:0001300 \| Parkinsonism \| 1 HP:0000717 \| Autism \| 1 HP:0003701 \| Proximal limb muscle weakness \| 1 HP:0002621 \| Atherosclerosis \| 1 HP:0012819 \| Myocarditis \| 1 HP:0003256 \| Coagulopathy \| 1

Disease ID	643
Disease	celiac disease
Manually Symptom	(Waiting for update.)
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:86) C0011854 \| type 1 diabetes \| 32 C0011849 \| diabetes mellitus \| 18 C0024299 \| lymphoma \| 17 C0011991 \| diarrhea \| 14 C0004364 \| autoimmune diseases \| 14 C0002871 \| anemia \| 13 C0024523 \| malabsorption \| 10 C0878544 \| cardiomyopathy \| 9 C1839611 \| n syndrome \| 8 C0426576 \| gastrointestinal symptoms \| 8 C0014544 \| epilepsy \| 7 C0040128 \| thyroid disease \| 7 C0021831 \| enteropathy \| 7 C0162316 \| iron deficiency \| 6 C0029456 \| osteoporosis \| 6 C0079772 \| t-cell lymphoma \| 6 C0021390 \| inflammatory bowel disease \| 5 C0001418 \| adenocarcinoma \| 5 C0021359 \| infertility \| 4 C0796095 \| c syndrome \| 4 C0241910 \| autoimmune hepatitis \| 4 C0011570 \| depression \| 4 C0162538 \| iga deficiency \| 3 C0002871 \| anaemia \| 3 C0162316 \| iron-deficiency anemia \| 3 C0920350 \| autoimmune thyroiditis \| 3 C0010346 \| crohn's disease \| 3 C0278803 \| small bowel adenocarcinoma \| 3 C0752303 \| urological manifestations \| 3 C0023895 \| liver disease \| 2 C0554021 \| recurrent aphthous stomatitis \| 2 C0041782 \| deficiency anaemia \| 2 C0400936 \| autoimmune liver disease \| 2 C2242708 \| hypertransaminasemia \| 2 C0024523 \| intestinal malabsorption \| 2 C0030305 \| pancreatitis \| 2 C0037285 \| skin manifestations \| 2 C0079731 \| b-cell lymphoma \| 2 C0004364 \| autoimmune disorders \| 2 C0017661 \| iga nephropathy \| 2 C0004134 \| ataxia \| 2 C1283271 \| lymphocytic gastritis \| 2 C0024282 \| lymphocytosis \| 2 C0022951 \| lactose intolerance \| 2 C0027765 \| neurologic disorders \| 2 C0400821 \| microscopic colitis \| 2 C0456889 \| enteropathy-associated t-cell lymphoma \| 2 C0021843 \| intestinal obstruction \| 1 C0035579 \| rickets \| 1 C0011633 \| dermatomyositis \| 1 C0009450 \| infectious disease \| 1 C0041296 \| tuberculosis \| 1 C0497327 \| dementia \| 1 C0024305 \| non-hodgkin lymphoma \| 1 C0011616 \| contact dermatitis \| 1 C0162316 \| iron deficiency anemia \| 1 C0021933 \| intussusception \| 1 C0036202 \| sarcoidosis \| 1 C0026986 \| myelodysplastic syndrome \| 1 C0031039 \| pericardial effusion \| 1 C0263338 \| chronic urticaria \| 1 C0029458 \| postmenopausal osteoporosis \| 1 C2711227 \| liver steatosis \| 1 C0162429 \| nutritional deficiencies \| 1 C0005779 \| coagulopathy \| 1 C0836924 \| thrombocytosis \| 1 C0037274 \| dermatosis \| 1 C0030293 \| pancreatic insufficiency \| 1 C0042164 \| uveitis \| 1 C0004093 \| weakness \| 1 C0007758 \| cerebellar ataxia \| 1 C0029442 \| osteomalacia \| 1 C0019189 \| chronic hepatitis \| 1 C0027873 \| neuromyelitis optica \| 1 C2242595 \| mucosal atrophy \| 1 C0152025 \| polyneuropathy \| 1 C0267373 \| intestinal bleeding \| 1 C0017152 \| gastritis \| 1 C0008311 \| cholangitis \| 1 C0162316 \| sideropenic anaemia \| 1 C0272404 \| hyposplenism \| 1 C0042487 \| deep vein thrombosis \| 1 C0850024 \| gluten sensitivity \| 1 C0267963 \| exocrine pancreatic insufficiency \| 1 C0856761 \| budd-chiari syndrome \| 1 C0015672 \| fatigue \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:157)
snpId	pubmedId	geneId	geneSymbol	diseaseId	sourceId	sentence	score	Year	geneSymbol_dbSNP	CHROMOSOME	POS	REF	ALT
rs1033180	20190752	56940	DUSP22	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	NA	6	383546	C	T
rs1033180	20190752	3662	IRF4	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	NA	6	383546	C	T
rs10806425	20190752	6885	MAP3K7	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	BACH2	6	90216893	C	A
rs10806425	20190752	60468	BACH2	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.244734064	2010	BACH2	6	90216893	C	A
rs10806425	20190752	60468	BACH2	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.244734064	2010	BACH2	6	90216893	C	A
rs10903122	20190752	864	RUNX3	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	NA	1	24977085	A	G
rs10936599	20190752	55892	MYNN	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122367032	2010	MYNN	3	169774313	C	T
rs10936599	20190752	55892	MYNN	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	MYNN	3	169774313	C	T
rs11221332	20190752	2113	ETS1	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.242367032	2010	ETS1	11	128511079	C	T
rs11221332	20190752	2113	ETS1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.242367032	2010	ETS1	11	128511079	C	T
rs11552708	22136669	8741	TNFSF13	umls:C0007570	BeFree	A regulatory SNP in TNFSF13 (rs11552708) is associated with CD (p = 0.01, OR = 0.7).	0.000271442	2012	TNFSF13;TNFSF12-TNFSF13	17	7559238	G	A
rs11712165	20190752	56983	POGLUT1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	ARHGAP31;LOC105374061	3	119399949	T	G
rs11712165	20190752	57514	ARHGAP31	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122367032	2010	ARHGAP31;LOC105374061	3	119399949	T	G
rs11712165	20190752	941	CD80	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.125005506	2010	ARHGAP31;LOC105374061	3	119399949	T	G
rs11712165	20190752	57514	ARHGAP31	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	ARHGAP31;LOC105374061	3	119399949	T	G
rs1250552	20190752	57178	ZMIZ1	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.242367032	2010	ZMIZ1	10	79298270	A	G
rs1250552	20190752	57178	ZMIZ1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.242367032	2010	ZMIZ1	10	79298270	A	G
rs12727642	20190752	3604	TNFRSF9	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	NA	1	7986612	C	A
rs12727642	20190752	11315	PARK7	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	NA	1	7986612	C	A
rs12734338	23936387	4660	PPP1R12B	umls:C0007570	GWASCAT	A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.	0.120271442	2013	PPP1R12B	1	202500595	T	C
rs12928822	20190752	8651	SOCS1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	LOC105371082	16	11310036	C	T
rs12928822	20190752	5619	PRM1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	LOC105371082	16	11310036	C	T
rs12928822	20190752	4261	CIITA	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002638474	2010	LOC105371082	16	11310036	C	T
rs12928822	20190752	23274	CLEC16A	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	LOC105371082	16	11310036	C	T
rs13003464	20190752	5966	REL	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.004734064	2010	PUS10	2	60959694	A	G
rs13003464	20190752	130872	AHSA2	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	PUS10	2	60959694	A	G
rs13003464	20190752	150962	PUS10	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122638474	2010	PUS10	2	60959694	A	G
rs13003464	20190752	150962	PUS10	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122638474	2010	PUS10	2	60959694	A	G
rs13010713	20190752	101927156	LOC101927156	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.12	2010	LOC101927156	2	181131318	A	G
rs13010713	20190752	10477	UBE2E3	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	LOC101927156	2	181131318	A	G
rs13010713	20190752	3676	ITGA4	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	LOC101927156	2	181131318	A	G
rs13015714	18311140	8809	IL18R1	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.124734064	2008	IL18R1	2	102355405	G	T
rs13015714	18311140	9173	IL1RL1	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.004734064	2008	IL18R1	2	102355405	G	T
rs13015714	18311140	8809	IL18R1	umls:C0007570	GWASCAT	Newly identified genetic risk variants for celiac disease related to the immune response.	0.124734064	2008	IL18R1	2	102355405	G	T
rs13015714	18311140	8807	IL18RAP	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.020379342	2008	IL18R1	2	102355405	G	T
rs13015714	18311140	389015	SLC9A4	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.002367032	2008	IL18R1	2	102355405	G	T
rs13098911	20190752	1232	CCR3	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.014745076	2010	NA	3	46193709	C	T
rs13098911	20190752	1230	CCR1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.007372538	2010	NA	3	46193709	C	T
rs13098911	20190752	1234	CCR5	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.004734064	2010	NA	3	46193709	C	T
rs13098911	20190752	10803	CCR9	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.005362824	2010	NA	3	46193709	C	T
rs13098911	20190752	9034	CCRL2	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	NA	3	46193709	C	T
rs13098911	20190752	2829	XCR1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	NA	3	46193709	C	T
rs13151961	20190752	84162	KIAA1109	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.135373836	2010	KIAA1109	4	122194347	A	G
rs13151961	20190752	59067	IL21	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.14099817	2010	KIAA1109	4	122194347	A	G
rs13151961	24999842	84162	KIAA1109	umls:C0007570	GWASCAT	Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.	0.135373836	2014	KIAA1109	4	122194347	A	G
rs13151961	20190752	3558	IL2	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.020726728	2010	KIAA1109	4	122194347	A	G
rs13151961	20190752	84162	KIAA1109	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.135373836	2010	KIAA1109	4	122194347	A	G
rs13314993	20190752	1233	CCR4	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	LOC105377022	3	32973977	G	T
rs1457092	20303373	4650	MYO9B	umls:C0007570	BeFree	To date, seven studies have provided evidence for an association between the gene encoding for myosin IXB (MYO9B) and celiac disease (CD), and inflammatory bowel diseases, including single nucleotide polymorphisms (SNPs) rs2305767, rs1457092, and rs2305764.	0.158615605	2010	MYO9B	19	17193427	C	A
rs1464510	18311140	4026	LPP	umls:C0007570	GWASCAT	Newly identified genetic risk variants for celiac disease related to the immune response.	0.130011012	2008	LPP	3	188394766	C	T,A
rs1464510	18311140	4026	LPP	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.130011012	2008	LPP	3	188394766	C	T,A
rs1464510	20190752	4026	LPP	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.130011012	2010	LPP	3	188394766	C	T,A
rs1464510	20190752	4026	LPP	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.130011012	2010	LPP	3	188394766	C	T,A
rs1545620	17087940	4650	MYO9B	umls:C0007570	BeFree	Common variation in MYO9B was associated with susceptibility to inflammatory bowel disease in all 3 cohorts examined (most associated SNP, rs1545620; meta-analysis P = 1.9 x 10(-6); odds ratio, 1.2), with the same alleles showing association as reported for celiac disease.	0.158615605	2006	MYO9B	19	17192965	T	G
rs1545620	17087940	5079	PAX5	umls:C0007570	BeFree	Common variation in MYO9B was associated with susceptibility to inflammatory bowel disease in all 3 cohorts examined (most associated SNP, rs1545620; meta-analysis P = 1.9 x 10(-6); odds ratio, 1.2), with the same alleles showing association as reported for celiac disease.	0.000271442	2006	MYO9B	19	17192965	T	G
rs1599796	19240061	941	CD80	umls:C0007570	GAD	[Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling.]	0.125005506	2009	CD80	3	119525087	G	A
rs17035378	20190752	5341	PLEK	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	PLEK;LOC101927723	2	68371823	T	C
rs17035378	20190752	5341	PLEK	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122367032	2010	PLEK;LOC101927723	2	68371823	T	C
rs1729657	19240061	84542	KIAA1841	umls:C0007570	GAD	[Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling.]	0.002367032	2009	KIAA1841	2	61076867	A	G
rs1738074	18311140	117289	TAGAP	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.132378044	2008	TAGAP;LOC105378082	6	159044945	T	C
rs1738074	20190752	117289	TAGAP	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.132378044	2010	TAGAP;LOC105378082	6	159044945	T	C
rs1738074	18311140	117289	TAGAP	umls:C0007570	GWASCAT	Newly identified genetic risk variants for celiac disease related to the immune response.	0.132378044	2008	TAGAP;LOC105378082	6	159044945	T	C
rs1738074	20190752	117289	TAGAP	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.132378044	2010	TAGAP;LOC105378082	6	159044945	T	C
rs17810546	20190752	3592	IL12A	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.013192369	2010	IL12A-AS1	3	159947262	A	G
rs17810546	18311140	101928376	IL12A-AS1	umls:C0007570	GWASCAT	Newly identified genetic risk variants for celiac disease related to the immune response.	0.12	2008	IL12A-AS1	3	159947262	A	G
rs17810546	18311140	3592	IL12A	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.013192369	2008	IL12A-AS1	3	159947262	A	G
rs17810546	18311140	29970	SCHIP1	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.002638474	2008	IL12A-AS1	3	159947262	A	G
rs17810546	20190752	101928376	IL12A-AS1	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.12	2010	IL12A-AS1	3	159947262	A	G
rs1799945	12145797	3077	HFE	umls:C0007570	BeFree	Polymerase chain reaction amplification using sequence-specific primers capable of identifying the 2 HFE gene mutations (H63D and C282Y) and the HLA class I and II alleles was used to type 145 white patients with celiac disease and 187 matched controls.	0.008186863	2002	HFE	6	26090951	C	G
rs1800562	12145797	3077	HFE	umls:C0007570	BeFree	Polymerase chain reaction amplification using sequence-specific primers capable of identifying the 2 HFE gene mutations (H63D and C282Y) and the HLA class I and II alleles was used to type 145 white patients with celiac disease and 187 matched controls.	0.008186863	2002	HFE	6	26092913	G	A
rs1800562	15929194	3077	HFE	umls:C0007570	BeFree	Occult CD may compensate for increased DMT1 expression in a specific subset of individuals with homozygous C282Y mutations in the hemochromatosis (HFE) gene, thus contributing to the low penetrance of HH.	0.008186863	2005	HFE	6	26092913	G	A
rs1801133	21688148	4524	MTHFR	umls:C0007570	BeFree	Recently, a possible excess in the frequency of the MTHFR c.677C>T (rs1801133) gene variant in CD patients was reported.	0.00554839	2012	MTHFR	1	11796321	G	A
rs1801274	19140833	2214	FCGR3A	umls:C0007570	BeFree	We studied the FcgammaRIIaA519G (rs1801274) and FcgammaRIIIaA559C (rs396991) single nucleotide polymorphisms in celiac disease families from Hungary and Finland and in celiac disease case-control materials from Hungary and Italy.	0.008001298	2009	FCGR2A	1	161509955	A	G
rs1893217	20190752	5771	PTPN2	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122367032	2010	PTPN2	18	12809341	A	G
rs1893217	20190752	5771	PTPN2	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	PTPN2	18	12809341	A	G
rs2074404	20190752	7473	WNT3	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122367032	2010	WNT3	17	46788073	T	G
rs2074404	20190752	7473	WNT3	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	WNT3	17	46788073	T	G
rs2187668	20190752	3117	HLA-DQA1	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.344489358	2010	HLA-DQA1	6	32638107	C	T
rs2187668	17558408	3117	HLA-DQA1	umls:C0007570	GWASCAT	A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.	0.344489358	2007	HLA-DQA1	6	32638107	C	T
rs2298428	20190752	7332	UBE2L3	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	YDJC	22	21628603	C	T
rs2298428	20190752	150223	YDJC	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122367032	2010	YDJC	22	21628603	C	T
rs2298428	20190752	150223	YDJC	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	YDJC	22	21628603	C	T
rs2305764	20303373	4650	MYO9B	umls:C0007570	BeFree	To date, seven studies have provided evidence for an association between the gene encoding for myosin IXB (MYO9B) and celiac disease (CD), and inflammatory bowel diseases, including single nucleotide polymorphisms (SNPs) rs2305767, rs1457092, and rs2305764.	0.158615605	2010	MYO9B	19	17203024	G	A
rs2305767	20303373	4650	MYO9B	umls:C0007570	BeFree	To date, seven studies have provided evidence for an association between the gene encoding for myosin IXB (MYO9B) and celiac disease (CD), and inflammatory bowel diseases, including single nucleotide polymorphisms (SNPs) rs2305767, rs1457092, and rs2305764.	0.158615605	2010	MYO9B	19	17183487	C	T
rs2327832	19240061	167826	OLIG3	umls:C0007570	BeFree	We identified two novel coeliac disease risk regions: 6q23.3 (OLIG3-TNFAIP3) and 2p16.1 (REL), both of which reached genome-wide significance in the combined analysis of all 2987 cases and 5273 controls (rs2327832 p = 1.3 x 10(-08), and rs842647 p = 5.2 x 10(-07)).	0.002638474	2009	NA	6	137651931	A	G
rs2327832	20190752	7128	TNFAIP3	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002909916	2010	NA	6	137651931	A	G
rs2327832	20190752	167826	OLIG3	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002638474	2010	NA	6	137651931	A	G
rs2474619	24999842	60468	BACH2	umls:C0007570	GWASCAT	Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.	0.244734064	2014	BACH2	6	90170316	C	A
rs2476601	18194365	26191	PTPN22	umls:C0007570	BeFree	The functional R620W variant of the PTPN22 gene is associated with celiac disease.	0.008458305	2008	PTPN22;AP4B1-AS1	1	113834946	A	G
rs2476601	15759012	26191	PTPN22	umls:C0007570	GAD	[Altogether, we have provided further evidence of an association between autoimmune diseases and the 1858C>T polymorphism in PTPN22.]	0.008458305	2005	PTPN22;AP4B1-AS1	1	113834946	A	G
rs2476601	16760194	26191	PTPN22	umls:C0007570	BeFree	This meta-analysis showed the association between the T-allele and the T/T genotype and JIA (OR = 1.34, P = 0.03; OR = 1.97, P = 0.02) but did not reveal the association between the PTPN22 C1858T polymorphism and IBD, psoriasis, multiple sclerosis, Addison's disease and Celiac disease.	0.008458305	2007	PTPN22;AP4B1-AS1	1	113834946	A	G
rs2762051	20190752	145165	ST13P4	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	DLEU1	13	50261579	C	T
rs2762051	20190752	10301	DLEU1	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.12	2010	DLEU1	13	50261579	C	T
rs2816316	18311140	431704	RGS21	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.004734064	2008	LOC105371664	1	192567683	C	A
rs2816316	18311140	5996	RGS1	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.012649486	2008	LOC105371664	1	192567683	C	A
rs2816316	20190752	5996	RGS1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.012649486	2010	LOC105371664	1	192567683	C	A
rs2816316	20190752	431704	RGS21	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.004734064	2010	LOC105371664	1	192567683	C	A
rs296547	20190752	647215	MROH3P	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	MROH3P	1	200923009	T	C
rs35829419	21245836	22861	NLRP1	umls:C0007570	BeFree	The missense variation Q705K in CIAS1/NALP3/NLRP3 gene and an NLRP1 haplotype are associated with celiac disease.	0.002638474	2011	NLRP3	1	247425556	C	A
rs35829419	21245836	114548	NLRP3	umls:C0007570	BeFree	The missense variation Q705K in CIAS1/NALP3/NLRP3 gene and an NLRP1 haplotype are associated with celiac disease.	0.003181358	2011	NLRP3	1	247425556	C	A
rs3748816	20190752	79258	MMEL1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	MMEL1	1	2595307	A	G
rs3748816	20190752	79258	MMEL1	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122367032	2010	MMEL1	1	2595307	A	G
rs3748816	20190752	8764	TNFRSF14	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122638474	2010	MMEL1	1	2595307	A	G
rs396991	19140833	2214	FCGR3A	umls:C0007570	BeFree	We studied the FcgammaRIIaA519G (rs1801274) and FcgammaRIIIaA559C (rs396991) single nucleotide polymorphisms in celiac disease families from Hungary and Finland and in celiac disease case-control materials from Hungary and Italy.	0.008001298	2009	FCGR3A	1	161544752	A	G,C
rs4675374	20190752	101927840	LOC101927840	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.12	2010	ICOS;LOC101927840	2	203937855	T	C
rs4675374	20190752	940	CD28	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.014092571	2010	ICOS;LOC101927840	2	203937855	T	C
rs4675374	20190752	29851	ICOS	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.133735253	2010	ICOS;LOC101927840	2	203937855	T	C
rs4675374	20190752	29851	ICOS	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.133735253	2010	ICOS;LOC101927840	2	203937855	T	C
rs4819388	20190752	23308	ICOSLG	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.242367032	2010	ICOSLG	21	44227538	T	C
rs4819388	20190752	23308	ICOSLG	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.242367032	2010	ICOSLG	21	44227538	T	C
rs4899260	20190752	677	ZFP36L1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	LOC105370548	14	68811487	C	T
rs531930	24999842	154215	NKAIN2	umls:C0007570	GWASCAT	Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.	0.12	2014	NKAIN2	6	124422361	A	G
rs5979785	20190752	51311	TLR8	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	NA	X	12953405	C	T
rs5979785	20190752	51284	TLR7	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	NA	X	12953405	C	T
rs6441961	18311140	100131327	UQCRC2P1	umls:C0007570	GWASCAT	Newly identified genetic risk variants for celiac disease related to the immune response.	0.12	2008	NA	3	46310893	T	C
rs6441961	18311140	1230	CCR1	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.007372538	2008	NA	3	46310893	T	C
rs6441961	18311140	1232	CCR3	umls:C0007570	GAD	[Type 1 diabetes and celiac disease share HLA-DQ, IL2-IL21, CCR3 and SH2B3 risk regions.]	0.014745076	2008	NA	3	46310893	T	C
rs653178	20190752	6311	ATXN2	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.127372538	2010	ATXN2	12	111569952	C	T
rs653178	18311140	10019	SH2B3	umls:C0007570	GAD	[Type 1 diabetes and celiac disease share HLA-DQ, IL2-IL21, CCR3 and SH2B3 risk regions.]	0.133192369	2008	ATXN2	12	111569952	C	T
rs653178	18311140	6311	ATXN2	umls:C0007570	GWASCAT	Newly identified genetic risk variants for celiac disease related to the immune response.	0.127372538	2008	ATXN2	12	111569952	C	T
rs653178	18311140	6311	ATXN2	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.127372538	2008	ATXN2	12	111569952	C	T
rs653178	25893417	10019	SH2B3	umls:C0007570	BeFree	One SNP (rs653178 at the SH2B3/ATXN2 locus) displayed study-wise statistically significant association with CAD with directionality consistent effects on celiac disease and CAD.	0.133192369	2015	ATXN2	12	111569952	C	T
rs653178	20190752	6311	ATXN2	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.127372538	2010	ATXN2	12	111569952	C	T
rs653178	20190752	10019	SH2B3	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.133192369	2010	ATXN2	12	111569952	C	T
rs653178	25893417	6311	ATXN2	umls:C0007570	BeFree	One SNP (rs653178 at the SH2B3/ATXN2 locus) displayed study-wise statistically significant association with CAD with directionality consistent effects on celiac disease and CAD.	0.127372538	2015	ATXN2	12	111569952	C	T
rs6691768	20190752	4774	NFIA	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122367032	2010	NFIA	1	61326191	G	A
rs6691768	20190752	4774	NFIA	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	NFIA	1	61326191	G	A
rs6806528	20190752	23150	FRMD4B	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122638474	2010	FRMD4B	3	69203748	C	T
rs6806528	20190752	23150	FRMD4B	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122638474	2010	FRMD4B	3	69203748	C	T
rs6822844	17999365	59067	IL21	umls:C0007570	BeFree	Recently, association of celiac disease with common single-nucleotide polymorphism (SNP) variants in an extensive linkage-disequilibrium block of 480 kb containing the KIAA1109, Tenr, IL2, and IL21 genes has been demonstrated in three independent populations (rs6822844P combined=1.3 x 10(-14)).	0.14099817	2007	NA	4	122588266	G	T
rs6822844	17558408	84162	KIAA1109	umls:C0007570	GAD	[A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.]	0.135373836	2007	NA	4	122588266	G	T
rs6822844	18311140	59067	IL21	umls:C0007570	GAD	[Type 1 diabetes and celiac disease share HLA-DQ, IL2-IL21, CCR3 and SH2B3 risk regions.]	0.14099817	2008	NA	4	122588266	G	T
rs6822844	18311140	132612	ADAD1	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.007458414	2008	NA	4	122588266	G	T
rs6822844	17558408	59067	IL21	umls:C0007570	GAD	[A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.]	0.14099817	2007	NA	4	122588266	G	T
rs6822844	18311140	3558	IL2	umls:C0007570	GAD	[Type 1 diabetes and celiac disease share HLA-DQ, IL2-IL21, CCR3 and SH2B3 risk regions.]	0.020726728	2008	NA	4	122588266	G	T
rs6822844	17558408	3558	IL2	umls:C0007570	GAD	[A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.]	0.020726728	2007	NA	4	122588266	G	T
rs6822844	17999365	84162	KIAA1109	umls:C0007570	BeFree	Recently, association of celiac disease with common single-nucleotide polymorphism (SNP) variants in an extensive linkage-disequilibrium block of 480 kb containing the KIAA1109, Tenr, IL2, and IL21 genes has been demonstrated in three independent populations (rs6822844P combined=1.3 x 10(-14)).	0.135373836	2007	NA	4	122588266	G	T
rs6822844	17999365	3558	IL2	umls:C0007570	BeFree	Recently, association of celiac disease with common single-nucleotide polymorphism (SNP) variants in an extensive linkage-disequilibrium block of 480 kb containing the KIAA1109, Tenr, IL2, and IL21 genes has been demonstrated in three independent populations (rs6822844P combined=1.3 x 10(-14)).	0.020726728	2007	NA	4	122588266	G	T
rs6822844	18311140	84162	KIAA1109	umls:C0007570	GAD	[Newly identified genetic risk variants for celiac disease related to the immune response.]	0.135373836	2008	NA	4	122588266	G	T
rs6974491	20190752	9844	ELMO1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122367032	2010	ELMO1	7	37334906	G	A
rs6974491	20190752	9844	ELMO1	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122367032	2010	ELMO1	7	37334906	G	A
rs802734	20190752	5796	PTPRK	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002638474	2010	NA	6	127957653	A	T,G
rs802734	23820479	387357	THEMIS	umls:C0007570	BeFree	Our study confirmed the association of this region with CD in our population, but only the genotype of rs802734 showed some influence in the expression of THEMIS.	0.120271442	2013	NA	6	127957653	A	T,G
rs80356624	19345438	3767	KCNJ11	umls:C0007570	BeFree	Sulfonylurea treatment in a girl with neonatal diabetes (KCNJ11 R201H) and celiac disease: impact of low compliance to the gluten free diet.	0.000271442	2009	KCNJ11	11	17387490	C	T,A
rs8081319	24999842	31	ACACA	umls:C0007570	GWASCAT	Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.	0.12	2014	ACACA;C17orf78	17	37374139	A	G
rs8081319	24999842	284099	C17orf78	umls:C0007570	GWASCAT	Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.	0.12	2014	ACACA;C17orf78	17	37374139	A	G
rs842647	19240061	5966	REL	umls:C0007570	GAD	[Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling.]	0.004734064	2009	REL	2	60892336	G	A
rs842647	19240061	167826	OLIG3	umls:C0007570	BeFree	We identified two novel coeliac disease risk regions: 6q23.3 (OLIG3-TNFAIP3) and 2p16.1 (REL), both of which reached genome-wide significance in the combined analysis of all 2987 cases and 5273 controls (rs2327832 p = 1.3 x 10(-08), and rs842647 p = 5.2 x 10(-07)).	0.002638474	2009	REL	2	60892336	G	A
rs859637	20190752	356	FASLG	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	LOC105371617	1	172741860	T	C
rs859637	20190752	7292	TNFSF4	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	LOC105371617	1	172741860	T	C
rs859637	20190752	8995	TNFSF18	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	LOC105371617	1	172741860	T	C
rs864537	20190752	919	CD247	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.122638474	2010	CD247	1	167442147	A	G
rs864537	20190752	919	CD247	umls:C0007570	GWASCAT	Multiple common variants for celiac disease influencing immune gene expression.	0.122638474	2010	CD247	1	167442147	A	G
rs917997	20190752	8807	IL18RAP	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.020379342	2010	NA	2	102454108	T	C
rs917997	20190752	8809	IL18R1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.124734064	2010	NA	2	102454108	T	C
rs917997	20190752	8808	IL1RL2	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.002367032	2010	NA	2	102454108	T	C
rs917997	20190752	9173	IL1RL1	umls:C0007570	GAD	[Multiple common variants for celiac disease influencing immune gene expression.]	0.004734064	2010	NA	2	102454108	T	C

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:666)
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
1	1066029	rs12145826	G	A	rs12145826	23936387	6.14E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12145826-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	1172907	rs715643	C	T	rs715643	23936387	2.61E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs715643-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	1981118	rs3795277	A	C	rs3795277	23936387	1.11E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3795277-A	Research Support, Non-U.S. Gov't	Comparative Study	T
1	2526746	rs3748816	A	G	rs3748816	20190752	3.00E-09	NA	1.12	[1.09-1.18]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
1	2539400	rs4445406	T	C	rs4445406	22057235	5.40E-12	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
1	2539400	rs4445406	T	C	rs4445406	23143596	5.40E-12	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
1	8046672	rs12727642	C	A	rs12727642	20190752	9.00E-08	NA	1.14	[1.09-1.20]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12727642-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
1	12661179	rs13376289	G	T	rs13376289	23936387	2.04E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13376289-G	Research Support, Non-U.S. Gov't	Comparative Study	G
1	13916997	rs10927905	T	C	rs10927905	23936387	2.53E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10927905-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	25289734	rs72657048	C	G	rs72657048	22057235	3.80E-06	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
1	25303576	rs10903122	A	G	rs10903122	20190752	2.00E-10	NA	1.12	[1.09-1.18]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
1	43751701	rs6697017	C	T	rs6697017	23936387	2.18E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6697017-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	43757762	rs34783763	T	C	rs34783763	23936387	2.52E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs34783763-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	56900270	rs875153	C	T	rs875153	17558408	4.30E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	NA
1	61791863	rs6691768	G	A	rs6691768	20190752	1.00E-07	NA	1.11	[1.06-1.15]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
1	62723566	rs958802	C	T	rs958802	23936387	1.45E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs958802-C	Research Support, Non-U.S. Gov't	Comparative Study	G
1	62848090	rs3949904	G	A	rs3949904	17558408	8.50E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
1	63767597	rs12747934	G	A	rs12747934	23936387	1.87E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12747934-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	63790503	rs6588025	T	C	rs6588025	23936387	3.96E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6588025-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	63793155	rs10749738	A	G	rs10749738	23936387	1.99E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10749738-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	64095111	rs855314	A	G	rs855314	23936387	5.94E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs855314-A	Research Support, Non-U.S. Gov't	Comparative Study	T
1	67416432	rs4655662	T	C	rs4655662	23936387	3.57E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4655662-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	67479598	rs2755242	T	C	rs2755242	23936387	3.58E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2755242-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	67487119	rs2065002	C	A	rs2065002	23936387	3.58E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2065002-A	Research Support, Non-U.S. Gov't	Comparative Study	C
1	67512903	rs1024229	G	T	rs1024229	23936387	1.53E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1024229-G	Research Support, Non-U.S. Gov't	Comparative Study	T
1	67512920	rs1024230	A	C	rs1024230	23936387	1.53E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1024230-A	Research Support, Non-U.S. Gov't	Comparative Study	C
1	67513574	rs2208577	A	C	rs2208577	23936387	3.00E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2208577-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	82379446	rs284227	C	T	rs284227	23936387	7.55E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs284227-C	Research Support, Non-U.S. Gov't	Comparative Study	A
1	82415199	rs385367	A	G	rs385367	23936387	7.65E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs385367-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	82438148	rs9438724	A	C	rs9438724	23936387	7.56E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9438724-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	83486078	rs1930278	A	G	rs1930278	23936387	4.47E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1930278-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	89072924	rs12024611	G	A	rs12024611	23936387	3.94E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12024611-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	89116300	rs7534720	T	C	rs7534720	23936387	5.44E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7534720-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	89126887	rs10493817	T	G	rs10493817	23936387	1.54E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10493817-G	Research Support, Non-U.S. Gov't	Comparative Study	T
1	89225976	rs430600	T	C	rs430600	23936387	1.72E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs430600-C	Research Support, Non-U.S. Gov't	Comparative Study	G
1	89265248	rs786911	T	C	rs786911	23936387	1.92E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs786911-C	Research Support, Non-U.S. Gov't	Comparative Study	G
1	89286673	rs786921	G	A	rs786921	23936387	2.87E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs786921-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	89307261	rs10801687	G	A	rs10801687	23936387	2.38E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10801687-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	105076810	rs316951	C	T	rs316951	23936387	2.48E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs316951-C	Research Support, Non-U.S. Gov't	Comparative Study	G
1	107874959	rs6672549	G	A	rs6672549	23936387	2.07E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6672549-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	108018847	rs96501	C	T	rs96501	23936387	1.79E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs96501-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	108356293	rs4612651	C	T	rs4612651	23936387	1.21E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4612651-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	108376302	rs7537000	A	G	rs7537000	23936387	2.11E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7537000-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	108402075	rs10494080	C	A	rs10494080	23936387	9.72E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10494080-A	Research Support, Non-U.S. Gov't	Comparative Study	C
1	113456368	rs11585690	A	C	rs11585690	23936387	4.87E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11585690-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	145545225	rs16827018	T	G	rs16827018	23936387	1.27E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs16827018-G	Research Support, Non-U.S. Gov't	Comparative Study	T
1	159319803	rs10218647	G	A	rs10218647	23936387	2.15E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10218647-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	166356784	rs12746568	T	C	rs12746568	23936387	2.06E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12746568-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	167198536	rs1021621	A	G	rs1021621	17558408	3.60E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	POU2F1
1	167392702	rs2949666	A	G	rs2949666	17558408	5.70E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	POU2F1
1	167411384	rs864537	A	G	rs864537	20190752	4.00E-07	NA	1.1	[1.06-1.15]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
1	168142489	rs4657739	C	T	rs4657739	23936387	2.98E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4657739-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	168149142	rs4657741	G	A	rs4657741	23936387	1.97E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4657741-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	168156627	rs2294253	C	T	rs2294253	23936387	4.87E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2294253-C	Research Support, Non-U.S. Gov't	Comparative Study	A
1	168159262	rs2235207	C	T	rs2235207	23936387	1.26E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2235207-C	Research Support, Non-U.S. Gov't	Comparative Study	A
1	168159890	rs1040404	G	A	rs1040404	23936387	8.24E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1040404-A	Research Support, Non-U.S. Gov't	Comparative Study	T
1	169762807	rs10489177	T	G	rs10489177	23936387	2.67E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10489177-G	Research Support, Non-U.S. Gov't	Comparative Study	A
1	169905053	rs10919271	G	A	rs10919271	23936387	2.39E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10919271-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	169985324	rs12123693	C	T	rs12123693	23936387	9.46E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12123693-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	169998200	rs10800495	C	T	rs10800495	23936387	7.18E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10800495-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	170002212	rs1415551	T	C	rs1415551	23936387	1.77E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1415551-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	170037624	rs12146137	C	T	rs12146137	23936387	9.64E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12146137-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	172681031	rs12068671	T	C	rs12068671	22057235	1.40E-10	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
1	172711000	rs859637	T	C	rs859637	20190752	2.00E-06	NA	1.1	[1.06-1.14]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs859637-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
1	172862234	rs9286879	A	G	rs9286879	24999842	8.25E-07	NA	1.29	[1.17-1.42]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	A	NA
1	172863948	rs2157453	G	A	rs2157453	24999842	8.00E-07	NA	1.29	[1.17-1.42]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	A,G	NA
1	172864652	rs12142280	T	A	rs12142280	22057235	8.30E-09	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
1	177451209	rs1885020	C	T	rs1885020	23936387	1.01E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1885020-C	Research Support, Non-U.S. Gov't	Comparative Study	G
1	185265149	rs10798004	G	A	rs10798004	23936387	1.81E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10798004-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	185430494	rs4323662	G	T	rs4323662	23936387	1.89E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4323662-G	Research Support, Non-U.S. Gov't	Comparative Study	T
1	192512559	rs72734930	G	A	rs72734930	22057235	3.70E-04	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
1	192536813	rs2816316	C	A	rs2816316	18311140	3.00E-11	NA	1.39	[1.26-1.53]	767 cases; 1,422 controls	NOPOP(2189)	ALL(2189)	NOPOP(2189)	ALL(2189)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2816316-C	Research Support, Non-U.S. Gov't	G	NA
1	192536813	rs2816316	C	A	rs2816316	20190752	2.00E-17	NA	1.25	[1.19-1.32]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
1	192541472	rs1359062	C	G	rs1359062	22057235	2.50E-25	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
1	192547052	rs10921202	G	T	rs10921202	23936387	3.96E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10921202-G	Research Support, Non-U.S. Gov't	Comparative Study	G
1	200881392	rs10800746	C	T	rs10800746	22057235	2.60E-08	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
1	200892137	rs296547	T	C	rs296547	20190752	4.00E-09	NA	1.12	[1.09-1.16]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
1	201594665	rs2068824	T	C	rs2068824	23936387	6.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2068824-C	Research Support, Non-U.S. Gov't	Comparative Study	G
1	202390914	rs12734001	C	T	rs12734001	23936387	2.32E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12734001-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	202469723	rs12734338	T	C	rs12734338	23936387	3.00E-07	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12734338-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	206668593	rs944775	T	C	rs944775	23936387	5.81E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs944775-C	Research Support, Non-U.S. Gov't	Comparative Study	A
1	206669958	rs15672	G	A	rs15672	23936387	6.81E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs15672-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	206676331	rs3860295	G	A	rs3860295	23936387	1.16E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3860295-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	209092473	rs10157571	C	T	rs10157571	23936387	2.24E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10157571-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	216080130	rs11120695	G	T	rs11120695	23936387	5.91E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11120695-G	Research Support, Non-U.S. Gov't	Comparative Study	G
1	218556297	rs10482751	T	C	rs10482751	23936387	2.32E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10482751-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	218559475	rs12029576	C	A	rs12029576	23936387	1.99E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12029576-A	Research Support, Non-U.S. Gov't	Comparative Study	C
1	222032485	rs12144971	C	T	rs12144971	23936387	6.26E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12144971-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	222039055	rs4240931	C	T	rs4240931	23936387	6.26E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4240931-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	222055403	rs11811613	A	G	rs11811613	23936387	2.16E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11811613-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	222109518	rs2790760	G	A	rs2790760	23936387	3.77E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2790760-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	225528183	rs3856145	C	A	rs3856145	23936387	2.76E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3856145-A	Research Support, Non-U.S. Gov't	Comparative Study	C
1	230688466	rs11122534	A	G	rs11122534	23936387	2.77E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11122534-A	Research Support, Non-U.S. Gov't	Comparative Study	A
1	232415093	rs11803212	G	A	rs11803212	23936387	1.29E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11803212-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	245008115	rs11579106	C	T	rs11579106	23936387	5.52E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11579106-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	247450565	rs12023478	C	T	rs12023478	23936387	1.63E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12023478-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	247471121	rs12023326	T	C	rs12023326	23936387	2.13E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12023326-C	Research Support, Non-U.S. Gov't	Comparative Study	T
1	247486736	rs6426239	C	T	rs6426239	23936387	2.13E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6426239-C	Research Support, Non-U.S. Gov't	Comparative Study	C
1	247490707	rs6690864	G	A	rs6690864	23936387	2.15E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6690864-A	Research Support, Non-U.S. Gov't	Comparative Study	G
1	247491143	rs10924987	C	T	rs10924987	23936387	9.91E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10924987-C	Research Support, Non-U.S. Gov't	Comparative Study	C
2	3508994	rs9798096	C	T	rs9798096	23936387	2.50E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9798096-C	Research Support, Non-U.S. Gov't	Comparative Study	C
2	7583311	rs7608732	A	C	rs7608732	23936387	2.40E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7608732-A	Research Support, Non-U.S. Gov't	Comparative Study	C
2	23606030	rs13397583	C	T	rs13397583	17558408	2.20E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	C	NA
2	30445322	rs1355208	A	G	rs1355208	17558408	3.40E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	NA
2	31415054	rs17010928	G	A	rs17010928	23936387	2.65E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17010928-A	Research Support, Non-U.S. Gov't	Comparative Study	G
2	38723049	rs13424546	G	A	rs13424546	23936387	6.33E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13424546-A	Research Support, Non-U.S. Gov't	Comparative Study	G
2	61186829	rs13003464	A	G	rs13003464	20190752	4.00E-13	NA	1.15	[1.11-1.20]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13003464-G	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
2	61186829	rs13003464	A	G	rs13003464	22057235	4.30E-16	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	61186829	rs13003464	A	G	rs13003464	23143596	4.30E-16	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
2	68598955	rs17035378	T	C	rs17035378	20190752	8.00E-09	NA	1.14	[1.09-1.19]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
2	68645560	rs10167650	T	G	rs10167650	22057235	1.30E-04	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	88513131	rs7590305	C	T	rs7590305	23936387	1.39E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7590305-C	Research Support, Non-U.S. Gov't	Comparative Study	C
2	102971865	rs13015714	G	T	rs13015714	18311140	4.00E-09		1.28	[1.18-1.39]	767 cases; 1,422 controls	NOPOP(2189)	ALL(2189)	NOPOP(2189)	ALL(2189)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13015714-C	Research Support, Non-U.S. Gov't	T	NA
2	103070568	rs917997	T	C	rs917997	17558408	6.80E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
2	103070568	rs917997	T	C	rs917997	20190752	1.00E-15	NA	1.19	[1.14-1.25]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs917997-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
2	103086770	rs990171	A	C	rs990171	22057235	1.20E-16	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	106076110	rs10203748	T	C	rs10203748	23936387	1.17E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10203748-C	Research Support, Non-U.S. Gov't	Comparative Study	T
2	112213244	rs1900710	C	T	rs1900710	23936387	2.50E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1900710-C	Research Support, Non-U.S. Gov't	Comparative Study	A
2	115622199	rs13007523	G	A	rs13007523	23936387	5.78E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13007523-A	Research Support, Non-U.S. Gov't	Comparative Study	G
2	115638290	rs13000828	G	A	rs13000828	23936387	1.40E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13000828-A	Research Support, Non-U.S. Gov't	Comparative Study	G
2	136555659	rs2322659	T	C	rs2322659	17558408	8.60E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	LCT
2	150508359	rs1526284	T	G	rs1526284	23936387	1.71E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1526284-G	Research Support, Non-U.S. Gov't	Comparative Study	T
2	173217091	rs4972809	A	G	rs4972809	23936387	2.16E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4972809-A	Research Support, Non-U.S. Gov't	Comparative Study	A
2	173217889	rs4972810	A	G	rs4972810	23936387	1.93E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4972810-A	Research Support, Non-U.S. Gov't	Comparative Study	G
2	181996045	rs13010713	A	G	rs13010713	20190752	5.00E-11	NA	1.13	[1.09-1.18]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13010713-G	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
2	182007800	rs1018326	T	C	rs1018326	22057235	3.10E-16	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	191723719	rs6741418	C	T	rs6741418	23936387	5.62E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6741418-C	Research Support, Non-U.S. Gov't	Comparative Study	C
2	191913034	rs6715106	A	G	rs6715106	22057235	8.40E-09	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	191913034	rs6715106	A	G	rs6715106	23143596	8.40E-09	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
2	191948637	rs12998748	G	A,C,T	rs12998748	22057235	2.60E-04	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	191948637	rs12998748	G	A,C,T	rs12998748	23143596	0.00026	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
2	191973563	rs6752770	A	G	rs6752770	22057235	1.30E-06	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	191973563	rs6752770	A	G	rs6752770	23143596	0.0000013	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
2	193724080	rs17654201	C	T	rs17654201	17558408	3.50E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	C	NA
2	195581699	rs801298	T	C	rs801298	23936387	5.49E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs801298-C	Research Support, Non-U.S. Gov't	Comparative Study	G
2	196309536	rs1542865	C	A	rs1542865	17558408	7.20E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
2	199657020	rs7587759	C	T	rs7587759	23936387	2.32E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7587759-C	Research Support, Non-U.S. Gov't	Comparative Study	T
2	204459961	rs10207814	C	T	rs10207814	22057235	1.30E-04	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	204459961	rs10207814	C	T	rs10207814	23143596	0.00013	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
2	204610396	rs1980422	C	T	rs1980422	22057235	1.40E-15	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	204610396	rs1980422	C	T	rs1980422	23143596	1.40E-15	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
2	204753487	rs231757	T	G	rs231757	23936387	5.07E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs231757-G	Research Support, Non-U.S. Gov't	Comparative Study	C
2	204763044	rs10197319	G	A	rs10197319	23936387	6.20E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10197319-A	Research Support, Non-U.S. Gov't	Comparative Study	A
2	204765194	rs7607760	G	T	rs7607760	23936387	6.34E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7607760-G	Research Support, Non-U.S. Gov't	Comparative Study	G
2	204770054	rs34037980	A	G	rs34037980	22057235	1.60E-05	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
2	204770054	rs34037980	A	G	rs34037980	23143596	0.000016	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
2	204770803	rs12616245	A	G	rs12616245	23936387	9.16E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12616245-A	Research Support, Non-U.S. Gov't	Comparative Study	G
2	204777404	rs11890284	C	T	rs11890284	23936387	5.66E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11890284-C	Research Support, Non-U.S. Gov't	Comparative Study	T
2	204802578	rs4675374	T	C	rs4675374	20190752	6.00E-09	NA	1.14	[1.09-1.19]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4675374-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
2	215341890	rs7604827	C	T	rs7604827	23936387	2.62E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7604827-C	Research Support, Non-U.S. Gov't	Comparative Study	T
2	232190985	rs10498225	C	A	rs10498225	23936387	9.29E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10498225-A	Research Support, Non-U.S. Gov't	Comparative Study	C
2	235078194	rs11884879	G	A	rs11884879	23936387	1.11E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11884879-A	Research Support, Non-U.S. Gov't	Comparative Study	A
2	240571827	rs4852100	A	G	rs4852100	17558408	3.80E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	NA
2	241968979	rs4234102	A	G	rs4234102	23936387	7.50E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4234102-A	Research Support, Non-U.S. Gov't	Comparative Study	C
3	2402673	rs9862494	T	C	rs9862494	17558408	1.10E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	CNTN4
3	24643573	rs12631757	C	T	rs12631757	23936387	2.09E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12631757-C	Research Support, Non-U.S. Gov't	Comparative Study	T
3	24782701	rs13433781	C	T	rs13433781	23936387	1.16E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13433781-C	Research Support, Non-U.S. Gov't	Comparative Study	C
3	33015469	rs13314993	G	T	rs13314993	20190752	3.00E-09	NA	1.13	[1.08-1.17]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13314993-C	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
3	33037721	rs4678523	T	C	rs4678523	22057235	2.40E-07	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
3	36352364	rs2046000	A	C	rs2046000	23936387	9.42E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2046000-A	Research Support, Non-U.S. Gov't	Comparative Study	G
3	36354537	rs1871352	A	C	rs1871352	23936387	1.66E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1871352-A	Research Support, Non-U.S. Gov't	Comparative Study	G
3	36360999	rs1479146	A	G	rs1479146	23936387	2.58E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1479146-A	Research Support, Non-U.S. Gov't	Comparative Study	C
3	36373765	rs1871350	C	T	rs1871350	23936387	8.49E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1871350-C	Research Support, Non-U.S. Gov't	Comparative Study	A
3	36391710	rs1842149	T	G	rs1842149	23936387	1.91E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1842149-G	Research Support, Non-U.S. Gov't	Comparative Study	C
3	36403951	rs1993923	C	T	rs1993923	23936387	2.83E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1993923-C	Research Support, Non-U.S. Gov't	Comparative Study	G
3	36409601	rs2605393	T	G	rs2605393	23936387	6.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2605393-G	Research Support, Non-U.S. Gov't	Comparative Study	G
3	39248852	rs12632771	A	G	rs12632771	23936387	2.43E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12632771-A	Research Support, Non-U.S. Gov't	Comparative Study	A
3	46205686	rs7616215	C	T	rs7616215	22057235	8.60E-09	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
3	46235201	rs13098911	C	T	rs13098911	20190752	3.00E-17	NA	1.3	[1.23-1.39]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13098911-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
3	46281744	rs13096142	C	T	rs13096142	23936387	4.52E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13096142-C	Research Support, Non-U.S. Gov't	Comparative Study	C
3	46281744	rs13096142	C	T	rs13096142	24999842	4.00E-08	NA	1.3	[1.18-1.43]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	C	NA
3	46345611	rs11711054	G	A	rs11711054	23936387	6.41E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11711054-A	Research Support, Non-U.S. Gov't	Comparative Study	G
3	46345611	rs11711054	G	A	rs11711054	24999842	8.80E-08	NA	1.29	[1.17-1.41]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	G	NA
3	46352384	rs6441961	T	C	rs6441961	18311140	3.00E-07		1.21	[1.13-1.30]	767 cases; 1,422 controls	NOPOP(2189)	ALL(2189)	NOPOP(2189)	ALL(2189)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6441961-A	Research Support, Non-U.S. Gov't	C	NA
3	46352384	rs6441961	T	C	rs6441961	23936387	8.99E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6441961-C	Research Support, Non-U.S. Gov't	Comparative Study	C
3	46352384	rs6441961	T	C	rs6441961	24999842	6.63E-08	NA	1.29	[1.19-1.42]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	C	NA
3	46378025	rs2097282	C	T	rs2097282	22057235	1.10E-20	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
3	46484283	rs6441991	T	A	rs6441991	22057235	4.80E-05	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
3	57200758	rs4283545	C	A	rs4283545	23936387	2.16E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4283545-A	Research Support, Non-U.S. Gov't	Comparative Study	C
3	57347878	rs571879	C	T	rs571879	23936387	1.38E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs571879-C	Research Support, Non-U.S. Gov't	Comparative Study	G
3	69252899	rs6806528	C	T	rs6806528	20190752	2.00E-07	NA	1.19	[1.12-1.27]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6806528-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
3	70161591	rs7639059	A	C	rs7639059	23936387	2.18E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7639059-A	Research Support, Non-U.S. Gov't	Comparative Study	C
3	71980643	rs7631897	G	A	rs7631897	23936387	3.39E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7631897-A	Research Support, Non-U.S. Gov't	Comparative Study	G
3	73958469	rs5012667	T	C	rs5012667	23936387	1.62E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs5012667-C	Research Support, Non-U.S. Gov't	Comparative Study	T
3	105422844	rs2305037	C	T	rs2305037	23936387	2.54E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2305037-C	Research Support, Non-U.S. Gov't	Comparative Study	G
3	105447746	rs1867189	G	A	rs1867189	23936387	2.30E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1867189-A	Research Support, Non-U.S. Gov't	Comparative Study	G
3	105449793	rs9876767	T	G	rs9876767	23936387	1.95E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9876767-G	Research Support, Non-U.S. Gov't	Comparative Study	T
3	105449986	rs9880861	T	C	rs9880861	23936387	2.71E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9880861-C	Research Support, Non-U.S. Gov't	Comparative Study	C
3	116839289	rs1357103	C	T	rs1357103	23936387	1.42E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1357103-C	Research Support, Non-U.S. Gov't	Comparative Study	A
3	119118796	rs11712165	T	G	rs11712165	20190752	8.00E-09	NA	1.13	[1.08-1.17]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11712165-C	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
3	119123278	rs61579022	G	A	rs61579022	22057235	9.90E-09	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
3	126228953	rs1873388	G	A	rs1873388	23936387	1.63E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1873388-A	Research Support, Non-U.S. Gov't	Comparative Study	C
3	126230388	rs777488	T	C	rs777488	23936387	2.09E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs777488-C	Research Support, Non-U.S. Gov't	Comparative Study	G
3	159623559	rs1353248	C	T	rs1353248	22057235	9.80E-09	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
3	159637678	rs76830965	C	A	rs76830965	22057235	2.60E-27	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
3	159665050	rs17810546	A	G	rs17810546	18311140	1.00E-09		1.35	[1.23-1.49]	767 cases; 1,422 controls	NOPOP(2189)	ALL(2189)	NOPOP(2189)	ALL(2189)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17810546-G	Research Support, Non-U.S. Gov't	A	NA
3	159665050	rs17810546	A	G	rs17810546	20190752	4.00E-28	NA	1.36	[1.29-1.44]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17810546-G	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
3	159674928	rs2561288	T	C	rs2561288	22057235	8.10E-08	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
3	169492101	rs10936599	C	T	rs10936599	20190752	5.00E-07	NA	1.12	[1.07-1.16]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10936599-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
3	179012000	rs6762743	C	T	rs6762743	17558408	8.10E-07	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	C	NA
3	179017020	rs9290678	A	G	rs9290678	17558408	1.10E-06	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
3	181448558	rs12491867	G	A	rs12491867	23936387	2.52E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12491867-A	Research Support, Non-U.S. Gov't	Comparative Study	G
3	185920603	rs2268844	T	G	rs2268844	23936387	2.90E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2268844-G	Research Support, Non-U.S. Gov't	Comparative Study	A
3	188072513	rs9865818	A	G	rs9865818	23936387	1.77E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9865818-A	Research Support, Non-U.S. Gov't	Comparative Study	A
3	188087628	rs9851967	C	T	rs9851967	23936387	7.94E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9851967-C	Research Support, Non-U.S. Gov't	Comparative Study	C
3	188112554	rs1464510	C	A,G,T	rs1464510	17558408	9.00E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	LPP
3	188112554	rs1464510	C	A,G,T	rs1464510	18311140	5.00E-09		1.23	[1.15-1.32]	767 cases; 1,422 controls	NOPOP(2189)	ALL(2189)	NOPOP(2189)	ALL(2189)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1464510-A	Research Support, Non-U.S. Gov't	G	LPP
3	188112554	rs1464510	C	A,G,T	rs1464510	20190752	3.00E-40	NA	1.29	[1.25-1.34]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1464510-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
3	188119901	rs2030519	G	A	rs2030519	22057235	3.00E-49	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
3	188639695	rs17283813	G	A	rs17283813	23936387	1.62E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17283813-A	Research Support, Non-U.S. Gov't	Comparative Study	A
3	188711067	rs1879903	G	A	rs1879903	23936387	3.11E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1879903-A	Research Support, Non-U.S. Gov't	Comparative Study	G
3	192758191	rs9283662	T	C	rs9283662	23936387	1.99E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9283662-C	Research Support, Non-U.S. Gov't	Comparative Study	T
3	194539121	rs9837804	T	C	rs9837804	23936387	2.08E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9837804-C	Research Support, Non-U.S. Gov't	Comparative Study	T
3	196351215	rs1385331	C	T	rs1385331	23936387	7.78E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1385331-C	Research Support, Non-U.S. Gov't	Comparative Study	C
3	196375140	rs6766451	T	G	rs6766451	23936387	5.39E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6766451-G	Research Support, Non-U.S. Gov't	Comparative Study	G
4	2139047	rs554399	G	A	rs554399	23936387	8.49E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs554399-A	Research Support, Non-U.S. Gov't	Comparative Study	A
4	5162389	rs13128441	C	T	rs13128441	23936387	8.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13128441-C	Research Support, Non-U.S. Gov't	Comparative Study	C
4	15896341	rs727488	C	T	rs727488	23936387	1.71E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs727488-C	Research Support, Non-U.S. Gov't	Comparative Study	T
4	32125658	rs6554006	G	A	rs6554006	17558408	7.60E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	NA
4	32125671	rs6554007	T	G	rs6554007	17558408	2.70E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
4	32140046	rs4536982	G	A	rs4536982	17558408	3.30E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
4	32592949	rs11940562	C	T	rs11940562	23936387	1.16E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11940562-C	Research Support, Non-U.S. Gov't	Comparative Study	C
4	75746665	rs6854845	G	T	rs6854845	23936387	1.34E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6854845-G	Research Support, Non-U.S. Gov't	Comparative Study	T
4	78327333	rs7682075	G	A	rs7682075	23936387	9.17E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7682075-A	Research Support, Non-U.S. Gov't	Comparative Study	A
4	82432524	rs17005153	A	G	rs17005153	23936387	2.51E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17005153-A	Research Support, Non-U.S. Gov't	Comparative Study	A
4	89445906	rs4693959	G	T	rs4693959	23936387	1.57E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4693959-G	Research Support, Non-U.S. Gov't	Comparative Study	T
4	95868525	rs1373651	G	A	rs1373651	23936387	2.46E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1373651-A	Research Support, Non-U.S. Gov't	Comparative Study	T
4	95892711	rs1373649	G	A	rs1373649	23936387	1.94E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1373649-A	Research Support, Non-U.S. Gov't	Comparative Study	T
4	96226609	rs17433092	C	T	rs17433092	23936387	7.50E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17433092-C	Research Support, Non-U.S. Gov't	Comparative Study	C
4	100509321	rs17029173	T	G	rs17029173	23936387	7.65E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17029173-G	Research Support, Non-U.S. Gov't	Comparative Study	G
4	100539896	rs1032355	T	C	rs1032355	23936387	5.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1032355-C	Research Support, Non-U.S. Gov't	Comparative Study	A
4	101965295	rs10025768	G	A	rs10025768	23936387	1.03E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10025768-A	Research Support, Non-U.S. Gov't	Comparative Study	A
4	105566441	rs624909	G	T	rs624909	23936387	2.55E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs624909-G	Research Support, Non-U.S. Gov't	Comparative Study	T
4	109411079	rs6838036	C	A	rs6838036	23936387	1.62E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6838036-A	Research Support, Non-U.S. Gov't	Comparative Study	A
4	122984633	rs1997179	T	C	rs1997179	24999842	4.01E-09	NA	1.49	[1.30-1.69]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	T	NA
4	123010587	rs13132933	T	C	rs13132933	24999842	1.02E-09	NA	1.47	[1.30-1.67]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	T	NA
4	123038295	rs62323881	C	A	rs62323881	22057235	8.60E-05	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
4	123038295	rs62323881	C	A	rs62323881	23143596	0.000086	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
4	123073009	rs11938795	T	C	rs11938795	17558408	1.70E-04	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NA
4	123073009	rs11938795	T	C	rs11938795	24999842	9.56E-07	NA	1.3	[1.18-1.45]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	T	NA
4	123115502	rs13151961	A	G	rs13151961	17558408	1.30E-12	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	KIAA1109
4	123115502	rs13151961	A	G	rs13151961	20190752	2.00E-27	NA	1.35	[1.28-1.43]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
4	123115502	rs13151961	A	G	rs13151961	24999842	3.00E-11	NA	1.54	[1.37-1.75]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	A	KIAA1109
4	123218313	rs13119723	A	G	rs13119723	17558408	4.80E-11	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	KIAA1109
4	123228113	rs11734090	T	C	rs11734090	17558408	2.30E-04	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	KIAA1109
4	123228113	rs11734090	T	C	rs11734090	24999842	6.16E-07	NA	1.32	[1.18-1.45]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	T	KIAA1109
4	123263446	rs6851362	T	C	rs6851362	24999842	2.01E-07	NA	1.33	[1.19-1.47]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	T	KIAA1109
4	123341159	rs7684187	G	A	rs7684187	17558408	5.60E-04	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	ADAD1
4	123508501	rs12642902	G	A	rs12642902	17558408	3.30E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
4	123509421	rs6822844	G	T	rs6822844	17558408	1.00E-14	NA	1.59	[1.41-1.75]	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6822844-G	Research Support, Non-U.S. Gov't	G	NA
4	123509421	rs6822844	G	T	rs6822844	18311140	3.00E-13	NA	1.44	[1.30-1.58]	767 cases; 1,422 controls	NOPOP(2189)	ALL(2189)	NOPOP(2189)	ALL(2189)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6822844-C	Research Support, Non-U.S. Gov't	G	NA
4	123551114	rs13132308	A	G	rs13132308	22057235	1.90E-38	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
4	123551114	rs13132308	A	G	rs13132308	23143596	1.90E-38	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
4	123554707	rs6840978	C	T	rs6840978	17558408	1.10E-10	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	C	NA
4	123554707	rs6840978	C	T	rs6840978	24999842	7.92E-10	NA	1.45	[1.28-1.64]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	C	NA
4	137634874	rs1460160	G	A	rs1460160	23936387	5.92E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1460160-A	Research Support, Non-U.S. Gov't	Comparative Study	G
4	140824542	rs11733737	C	T	rs11733737	23936387	2.01E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11733737-C	Research Support, Non-U.S. Gov't	Comparative Study	C
4	140831781	rs1350036	C	T	rs1350036	23936387	1.66E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1350036-C	Research Support, Non-U.S. Gov't	Comparative Study	C
4	141022942	rs1402673	A	G	rs1402673	23936387	4.20E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1402673-A	Research Support, Non-U.S. Gov't	Comparative Study	G
4	158502750	rs6830776	C	T	rs6830776	23936387	9.68E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6830776-C	Research Support, Non-U.S. Gov't	Comparative Study	C
4	172904310	rs13122067	C	T	rs13122067	23936387	2.81E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13122067-C	Research Support, Non-U.S. Gov't	Comparative Study	C
4	173418304	rs6553634	A	G	rs6553634	23936387	3.30E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6553634-A	Research Support, Non-U.S. Gov't	Comparative Study	A
4	175097637	rs7661496	A	G	rs7661496	23936387	2.93E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7661496-A	Research Support, Non-U.S. Gov't	Comparative Study	G
4	175461530	rs2555639	T	C	rs2555639	23936387	1.32E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2555639-C	Research Support, Non-U.S. Gov't	Comparative Study	G
4	175462630	rs9990951	C	A	rs9990951	23936387	1.96E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9990951-A	Research Support, Non-U.S. Gov't	Comparative Study	A
4	189488734	rs1600203	T	C	rs1600203	17558408	9.20E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	LOC401164
5	4633984	rs10512743	G	A	rs10512743	23936387	8.20E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10512743-A	Research Support, Non-U.S. Gov't	Comparative Study	G
5	9204142	rs1805971	C	T	rs1805971	23936387	1.60E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1805971-C	Research Support, Non-U.S. Gov't	Comparative Study	A
5	16661282	rs7722385	C	T	rs7722385	23936387	1.80E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7722385-C	Research Support, Non-U.S. Gov't	Comparative Study	C
5	17018543	rs4374758	T	C	rs4374758	23936387	1.63E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4374758-C	Research Support, Non-U.S. Gov't	Comparative Study	C
5	27950483	rs30810	C	T	rs30810	23936387	8.95E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs30810-C	Research Support, Non-U.S. Gov't	Comparative Study	T
5	73559582	rs11738478	T	C	rs11738478	23936387	5.28E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11738478-C	Research Support, Non-U.S. Gov't	Comparative Study	C
5	86271618	rs1073933	T	C	rs1073933	23936387	1.99E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1073933-C	Research Support, Non-U.S. Gov't	Comparative Study	A
5	124490816	rs1866543	G	A	rs1866543	23936387	2.39E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1866543-A	Research Support, Non-U.S. Gov't	Comparative Study	G
5	138288530	rs17207814	G	A	rs17207814	23936387	4.21E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17207814-A	Research Support, Non-U.S. Gov't	Comparative Study	G
5	145131972	rs11740064	T	C	rs11740064	23936387	3.98E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11740064-C	Research Support, Non-U.S. Gov't	Comparative Study	T
5	150751557	rs13357969	A	G	rs13357969	17558408	9.30E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
5	150789051	rs7708940	A	G	rs7708940	17558408	5.40E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	NA
5	159391811	rs11953285	A	C	rs11953285	23936387	2.84E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11953285-A	Research Support, Non-U.S. Gov't	Comparative Study	A
5	172283930	rs13155834	A	G	rs13155834	23936387	1.20E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13155834-A	Research Support, Non-U.S. Gov't	Comparative Study	A
5	180214474	rs682828	C	T	rs682828	23936387	7.94E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs682828-C	Research Support, Non-U.S. Gov't	Comparative Study	A
6	383546	rs1033180	C	T	rs1033180	20190752	6.00E-08	NA	1.21	[1.13-1.29]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1033180-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
6	396321	rs12203592	C	T	rs12203592	22057235	2.60E-04	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
6	408079	rs1050976	C	T	rs1050976	22057235	1.80E-09	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
6	7330169	rs9379089	T	C	rs9379089	23936387	2.69E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9379089-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	16433223	rs4716071	G	A	rs4716071	23936387	1.90E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4716071-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	17755884	rs9396802	T	C	rs9396802	23936387	1.05E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9396802-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	19549868	rs4710911	A	C	rs4710911	23936387	2.22E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4710911-A	Research Support, Non-U.S. Gov't	Comparative Study	C
6	20418718	rs744143	G	A	rs744143	23936387	2.45E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs744143-A	Research Support, Non-U.S. Gov't	Comparative Study	C
6	22286012	rs1205961	A	G	rs1205961	23936387	3.65E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1205961-A	Research Support, Non-U.S. Gov't	Comparative Study	T
6	24042393	rs10946659	T	G	rs10946659	23936387	9.26E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10946659-G	Research Support, Non-U.S. Gov't	Comparative Study	T
6	24059407	rs9467027	C	T	rs9467027	23936387	2.10E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9467027-C	Research Support, Non-U.S. Gov't	Comparative Study	C
6	24078258	rs9460965	C	T	rs9460965	23936387	1.63E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9460965-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	24615063	rs7763790	G	A	rs7763790	23936387	2.91E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7763790-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	26286744	rs9358918	C	T	rs9358918	23936387	5.10E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9358918-C	Research Support, Non-U.S. Gov't	Comparative Study	C
6	26309908	rs10484439	G	A	rs10484439	23936387	2.85E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10484439-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	26313348	rs6923139	C	T	rs6923139	23936387	2.91E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6923139-C	Research Support, Non-U.S. Gov't	Comparative Study	C
6	26376832	rs13218591	T	C	rs13218591	23936387	5.39E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13218591-C	Research Support, Non-U.S. Gov't	Comparative Study	C,T
6	26463660	rs13195509	G	A	rs13195509	23936387	2.31E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13195509-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	32109979	rs204999	A	G	rs204999	23936387	7.95E-21	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs204999-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	32208324	rs424232	C	T	rs424232	23936387	5.00E-21	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs424232-C	Research Support, Non-U.S. Gov't	Comparative Study	G
6	32605884	rs2187668	C	T	rs2187668	17558408	1.00E-19	NA	7.04	[6.08-8.15]	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2187668-A	Research Support, Non-U.S. Gov't	G	HLA-DQA1
6	32605884	rs2187668	C	T	rs2187668	20190752	1.00E-50	NA	6.23	[5.95-6.52]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2187668-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
6	32651117	rs9275141	T	G	rs9275141	17558408	3.90E-16	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
6	32664960	rs9357152	A	G	rs9357152	17558408	5.20E-14	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	NA
6	36944479	rs9296204	T	C	rs9296204	23936387	3.20E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9296204-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	38757378	rs7756191	C	T	rs7756191	23936387	5.81E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7756191-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	41305976	rs10947963	G	A	rs10947963	23936387	1.13E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10947963-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	43791080	rs6458351	T	C	rs6458351	23936387	1.69E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6458351-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	47916225	rs1974051	A	G	rs1974051	23936387	5.12E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1974051-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	47923245	rs10485047	T	C	rs10485047	23936387	2.73E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10485047-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	52465451	rs6936059	G	T	rs6936059	17558408	1.80E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NA
6	57591840	rs7759896	C	T	rs7759896	23936387	2.55E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7759896-C	Research Support, Non-U.S. Gov't	Comparative Study	C
6	63174910	rs9351812	C	T	rs9351812	23936387	1.61E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9351812-C	Research Support, Non-U.S. Gov't	Comparative Study	C
6	63209941	rs2345981	G	A	rs2345981	23936387	1.76E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2345981-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	72330088	rs1889276	C	T	rs1889276	23936387	1.44E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1889276-C	Research Support, Non-U.S. Gov't	Comparative Study	C
6	72356780	rs6938557	G	A	rs6938557	23936387	2.35E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6938557-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	90809639	rs7753008	T	C	rs7753008	22057235	2.70E-07	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
6	90809639	rs7753008	T	C	rs7753008	23143596	0.00000027	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
6	90880035	rs2474619	C	A	rs2474619	24999842	2.00E-08	NA	1.28	[1.18-1.41]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	A	BACH2
6	90926612	rs10806425	C	A	rs10806425	20190752	4.00E-10	NA	1.13	[1.09-1.17]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10806425-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
6	91019304	rs1394220	A	C	rs1394220	24999842	5.30E-07	NA	1.25	[1.14-1.36]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	A	NA
6	92828724	rs4571541	G	A	rs4571541	17558408	2.80E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
6	92829488	rs4446534	G	A	rs4446534	17558408	3.30E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
6	99640610	rs7745052	G	A	rs7745052	23936387	8.44E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7745052-A	Research Support, Non-U.S. Gov't	Comparative Study	G
6	122981550	rs12209247	T	C	rs12209247	23936387	9.49E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12209247-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	124743507	rs531930	A	G	rs531930	24999842	5.00E-07	NA	1.3	[1.17-1.44]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	G	NKAIN2
6	128175722	rs10484716	A	G	rs10484716	17558408	6.80E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	THEMIS
6	128278798	rs802734	A	G	rs802734	20190752	3.00E-14	NA	1.17	[1.12-1.22]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs802734-G	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
6	128293562	rs55743914	C	T	rs55743914	22057235	1.10E-18	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
6	128294055	rs72975916	C	T	rs72975916	22057235	1.20E-05	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
6	129439995	rs12213754	A	G	rs12213754	23936387	1.35E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12213754-A	Research Support, Non-U.S. Gov't	Comparative Study	A
6	130827482	rs9402234	C	T	rs9402234	23936387	1.37E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9402234-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	131402814	rs13208443	G	T	rs13208443	23936387	4.44E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13208443-G	Research Support, Non-U.S. Gov't	Comparative Study	G
6	137973068	rs2327832	A	G	rs2327832	20190752	4.00E-19	NA	1.23	[1.17-1.28]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2327832-G	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
6	138002061	rs77027760	G	A	rs77027760	22057235	2.10E-07	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
6	138002061	rs77027760	G	A	rs77027760	23143596	0.00000021	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
6	138005515	rs17264332	A	G	rs17264332	22057235	5.00E-30	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
6	138005515	rs17264332	A	G	rs17264332	23143596	5.00E-30	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
6	145543523	rs551923	G	A	rs551923	23936387	9.97E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs551923-A	Research Support, Non-U.S. Gov't	Comparative Study	A
6	156673243	rs9397928	T	C	rs9397928	23936387	7.13E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9397928-C	Research Support, Non-U.S. Gov't	Comparative Study	T
6	159465977	rs1738074	T	C	rs1738074	18311140	7.00E-08		1.21	[1.13-1.30]	767 cases; 1,422 controls	NOPOP(2189)	ALL(2189)	NOPOP(2189)	ALL(2189)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1738074-A	Research Support, Non-U.S. Gov't	A	TAGAP
6	159465977	rs1738074	T	C	rs1738074	20190752	3.00E-15	NA	1.16	[1.12-1.21]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1738074-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
6	159465977	rs1738074	T	C	rs1738074	24999842	3.40E-08	NA	1.28	[1.18-1.40]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	A	TAGAP
6	159469574	rs182429	A	G	rs182429	22057235	8.50E-16	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
6	159469574	rs182429	A	G	rs182429	23143596	8.50E-16	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
6	159472295	rs212402	G	A	rs212402	24999842	8.00E-09	NA	1.31	[1.20-1.44]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	C	NA
6	159484776	rs169858	T	C	rs169858	24999842	1.27E-07	NA	1.29	[1.17-1.41]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	G	NA
6	159490436	rs212388	C	T	rs212388	24999842	1.82E-08	NA	1.29	[1.19-1.41]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	G	NA
6	159498267	rs1107943	T	C	rs1107943	22057235	2.80E-06	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
6	159498267	rs1107943	T	C	rs1107943	23143596	0.0000028	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
6	159514778	rs654690	T	C	rs654690	24999842	3.05E-08	NA	1.3	[1.18-1.42]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	G	NA
6	159515309	rs2249937	T	G	rs2249937	24999842	2.74E-07	NA	1.28	[1.16-1.40]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	C	NA
6	169559506	rs9294965	G	A	rs9294965	23936387	2.20E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9294965-A	Research Support, Non-U.S. Gov't	Comparative Study	G
7	3007393	rs7795713	C	T	rs7795713	23936387	1.76E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7795713-C	Research Support, Non-U.S. Gov't	Comparative Study	C
7	37374510	rs6974491	G	A	rs6974491	20190752	2.00E-07	NA	1.14	[1.09-1.20]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6974491-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
7	37418454	rs79758729	A	G	rs79758729	22057235	2.10E-08	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
7	37418454	rs79758729	A	G	rs79758729	23143596	0.000000021	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
7	76444648	rs2192268	T	G	rs2192268	23936387	2.54E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2192268-G	Research Support, Non-U.S. Gov't	Comparative Study	T
7	89195515	rs1072107	G	A	rs1072107	23936387	1.99E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1072107-A	Research Support, Non-U.S. Gov't	Comparative Study	G
7	98163939	rs817759	T	C	rs817759	23936387	1.46E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs817759-C	Research Support, Non-U.S. Gov't	Comparative Study	A,G
7	152595852	rs7795581	T	C	rs7795581	23936387	8.26E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7795581-C	Research Support, Non-U.S. Gov't	Comparative Study	T
7	154508225	rs10259988	G	A	rs10259988	23936387	5.87E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10259988-A	Research Support, Non-U.S. Gov't	Comparative Study	G
7	154508288	rs4960602	G	A	rs4960602	23936387	6.37E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4960602-A	Research Support, Non-U.S. Gov't	Comparative Study	A
7	156701918	rs11760288	G	A	rs11760288	23936387	2.06E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11760288-A	Research Support, Non-U.S. Gov't	Comparative Study	G
8	60290816	rs7004358	G	A	rs7004358	23936387	5.47E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7004358-A	Research Support, Non-U.S. Gov't	Comparative Study	G
8	61827676	rs12680914	G	T	rs12680914	23936387	2.46E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12680914-G	Research Support, Non-U.S. Gov't	Comparative Study	G
8	75096991	rs4385459	A	G	rs4385459	23936387	9.78E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4385459-A	Research Support, Non-U.S. Gov't	Comparative Study	G
8	75109785	rs2956060	A	G	rs2956060	23936387	2.84E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2956060-A	Research Support, Non-U.S. Gov't	Comparative Study	T
8	103138045	rs648119	A	G	rs648119	17558408	4.00E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NA
8	103524176	rs4734058	C	T	rs4734058	23936387	2.04E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4734058-C	Research Support, Non-U.S. Gov't	Comparative Study	C
8	116816440	rs12544542	G	A	rs12544542	23936387	5.60E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12544542-A	Research Support, Non-U.S. Gov't	Comparative Study	A
8	128108993	rs17832285	A	G	rs17832285	23936387	4.39E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17832285-A	Research Support, Non-U.S. Gov't	Comparative Study	A
8	129264060	rs10808568	A	C	rs10808568	22057235	2.20E-05	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
8	129264060	rs10808568	A	C	rs10808568	23143596	0.000022	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
8	129264589	rs9792269	A	G	rs9792269	20190752	3.00E-09	NA	1.14	[1.10-1.19]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
8	134027588	rs10505604	A	G	rs10505604	17558408	3.10E-06	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	TG
8	139504270	rs11166827	C	T	rs11166827	23936387	2.77E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11166827-C	Research Support, Non-U.S. Gov't	Comparative Study	C
8	142132965	rs1467073	A	G	rs1467073	23936387	2.45E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1467073-A	Research Support, Non-U.S. Gov't	Comparative Study	G
8	143145547	rs12334475	C	T	rs12334475	23936387	3.29E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12334475-C	Research Support, Non-U.S. Gov't	Comparative Study	C
9	1339391	rs4469515	A	G	rs4469515	17558408	4.60E-06	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
9	1878648	rs7862396	T	C	rs7862396	23936387	1.10E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7862396-C	Research Support, Non-U.S. Gov't	Comparative Study	T
9	2172235	rs10965086	A	G	rs10965086	23936387	8.87E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10965086-A	Research Support, Non-U.S. Gov't	Comparative Study	A
9	2495870	rs1571812	C	A	rs1571812	23936387	3.35E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1571812-A	Research Support, Non-U.S. Gov't	Comparative Study	C
9	16129630	rs1536689	A	G	rs1536689	23936387	1.52E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1536689-A	Research Support, Non-U.S. Gov't	Comparative Study	A
9	20346912	rs13296370	T	C	rs13296370	23936387	1.29E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13296370-C	Research Support, Non-U.S. Gov't	Comparative Study	T
9	20461775	rs13299141	T	C	rs13299141	23936387	3.65E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13299141-C	Research Support, Non-U.S. Gov't	Comparative Study	T
9	21565674	rs7033598	C	T	rs7033598	23936387	1.35E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7033598-C	Research Support, Non-U.S. Gov't	Comparative Study	T
9	26370564	rs451664	G	A	rs451664	23936387	9.97E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs451664-A	Research Support, Non-U.S. Gov't	Comparative Study	A
9	26371680	rs406058	G	A	rs406058	23936387	5.65E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs406058-A	Research Support, Non-U.S. Gov't	Comparative Study	T
9	26694184	rs7871815	G	A	rs7871815	23936387	2.95E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7871815-A	Research Support, Non-U.S. Gov't	Comparative Study	A
9	27341338	rs7041639	A	G	rs7041639	23936387	6.48E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7041639-A	Research Support, Non-U.S. Gov't	Comparative Study	A
9	28276698	rs13301122	G	A	rs13301122	17558408	3.80E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	LINGO2
9	79513254	rs12553751	G	A	rs12553751	23936387	2.77E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12553751-A	Research Support, Non-U.S. Gov't	Comparative Study	G
9	79794753	rs4012480	G	T	rs4012480	23936387	1.02E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4012480-G	Research Support, Non-U.S. Gov't	Comparative Study	A
9	79802986	rs12338283	G	A	rs12338283	23936387	7.98E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12338283-A	Research Support, Non-U.S. Gov't	Comparative Study	G
9	79846516	rs11145347	T	C	rs11145347	23936387	8.32E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11145347-C	Research Support, Non-U.S. Gov't	Comparative Study	T
9	79862502	rs10115162	T	C	rs10115162	23936387	1.03E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10115162-C	Research Support, Non-U.S. Gov't	Comparative Study	T,C
9	79891237	rs7030802	T	G	rs7030802	23936387	8.65E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7030802-G	Research Support, Non-U.S. Gov't	Comparative Study	T
9	79936415	rs17423984	A	G	rs17423984	23936387	9.42E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17423984-A	Research Support, Non-U.S. Gov't	Comparative Study	A
9	79954545	rs7025532	T	C	rs7025532	23936387	8.36E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7025532-C	Research Support, Non-U.S. Gov't	Comparative Study	T
9	79980974	rs10491843	A	C	rs10491843	23936387	9.28E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10491843-A	Research Support, Non-U.S. Gov't	Comparative Study	T
9	95541775	rs10992463	C	T	rs10992463	23936387	1.48E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10992463-C	Research Support, Non-U.S. Gov't	Comparative Study	C
9	106604233	rs7046385	T	C	rs7046385	23936387	9.99E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7046385-C	Research Support, Non-U.S. Gov't	Comparative Study	T
9	128957168	rs10987191	C	A	rs10987191	23936387	1.41E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10987191-A	Research Support, Non-U.S. Gov't	Comparative Study	C
9	132018506	rs11564091	C	T	rs11564091	23936387	1.69E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11564091-C	Research Support, Non-U.S. Gov't	Comparative Study	C
9	138474785	rs4842007	T	C	rs4842007	23936387	6.72E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4842007-C	Research Support, Non-U.S. Gov't	Comparative Study	T
9	139575487	rs9411216	G	A	rs9411216	23936387	8.39E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9411216-A	Research Support, Non-U.S. Gov't	Comparative Study	G
10	1416962	rs11250483	C	T	rs11250483	23936387	1.99E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11250483-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	1692796	rs7072699	C	T	rs7072699	23936387	2.76E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7072699-C	Research Support, Non-U.S. Gov't	Comparative Study	C
10	3230052	rs7093944	C	A	rs7093944	23936387	2.21E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7093944-A	Research Support, Non-U.S. Gov't	Comparative Study	A
10	6276574	rs1064891	T	C	rs1064891	17558408	2.70E-06	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	PFKFB3
10	6276743	rs1539234	G	A	rs1539234	17558408	4.60E-06	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	PFKFB3
10	6390192	rs2387397	G	C	rs2387397	22057235	1.90E-08	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
10	6390192	rs2387397	G	C	rs2387397	23143596	0.000000019	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
10	6401625	rs4558075	C	T	rs4558075	24999842	2.00E-07	NA	1.37	[1.22-1.54]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	T	NA
10	6402741	rs10796045	G	T	rs10796045	24999842	4.63E-07	NA	1.35	[1.20-1.52]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	T	NA
10	6631867	rs2435587	G	A	rs2435587	23936387	1.49E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2435587-A	Research Support, Non-U.S. Gov't	Comparative Study	A
10	17258799	rs1470379	C	T	rs1470379	23936387	1.45E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1470379-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	17279517	rs3249	C	T	rs3249	23936387	1.55E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3249-C	Research Support, Non-U.S. Gov't	Comparative Study	G
10	17285064	rs243013	A	C	rs243013	23936387	1.52E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs243013-A	Research Support, Non-U.S. Gov't	Comparative Study	G
10	17302891	rs911607	G	A	rs911607	23936387	2.56E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs911607-A	Research Support, Non-U.S. Gov't	Comparative Study	C
10	24230240	rs11013804	C	T	rs11013804	23936387	2.38E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11013804-C	Research Support, Non-U.S. Gov't	Comparative Study	A
10	24233614	rs4420167	A	G	rs4420167	23936387	2.60E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4420167-A	Research Support, Non-U.S. Gov't	Comparative Study	G
10	81058027	rs1250552	A	G	rs1250552	20190752	9.00E-10	NA	1.12	[1.09-1.16]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
10	81058027	rs1250552	A	G	rs1250552	22057235	8.00E-17	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
10	95330890	rs12415204	C	A	rs12415204	23936387	1.11E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12415204-A	Research Support, Non-U.S. Gov't	Comparative Study	C
10	100794359	rs10786497	T	C	rs10786497	23936387	1.44E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10786497-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	108679892	rs7079264	A	G	rs7079264	23936387	2.72E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7079264-A	Research Support, Non-U.S. Gov't	Comparative Study	G
10	108681669	rs7097380	G	A	rs7097380	23936387	2.27E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7097380-A	Research Support, Non-U.S. Gov't	Comparative Study	A,G
10	108685212	rs10509825	T	C	rs10509825	23936387	2.40E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10509825-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	108686065	rs10884381	C	T	rs10884381	23936387	7.30E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10884381-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	108688778	rs11193120	G	A	rs11193120	23936387	5.72E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11193120-A	Research Support, Non-U.S. Gov't	Comparative Study	A
10	108692152	rs10884387	C	T	rs10884387	23936387	6.78E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10884387-C	Research Support, Non-U.S. Gov't	Comparative Study	C
10	108698509	rs822076	C	T	rs822076	23936387	1.41E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs822076-C	Research Support, Non-U.S. Gov't	Comparative Study	C
10	108709195	rs822095	A	G	rs822095	23936387	9.46E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs822095-A	Research Support, Non-U.S. Gov't	Comparative Study	G
10	108710127	rs10786998	A	C	rs10786998	23936387	2.30E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10786998-A	Research Support, Non-U.S. Gov't	Comparative Study	C
10	108798092	rs17121941	A	G	rs17121941	23936387	7.34E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17121941-A	Research Support, Non-U.S. Gov't	Comparative Study	A
10	110286149	rs11194147	C	T	rs11194147	23936387	9.22E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11194147-C	Research Support, Non-U.S. Gov't	Comparative Study	C
10	117860851	rs17094083	T	C	rs17094083	23936387	2.35E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17094083-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	117861297	rs3781514	G	A	rs3781514	23936387	6.33E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3781514-A	Research Support, Non-U.S. Gov't	Comparative Study	G
10	119613610	rs10886159	T	C	rs10886159	23936387	7.00E-07	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10886159-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	119613633	rs4752123	T	C	rs4752123	23936387	2.17E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4752123-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	121290571	rs4752324	T	C	rs4752324	23936387	2.30E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4752324-C	Research Support, Non-U.S. Gov't	Comparative Study	C
10	124660458	rs7915165	G	A	rs7915165	23936387	1.47E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7915165-A	Research Support, Non-U.S. Gov't	Comparative Study	NA
10	124671655	rs7921647	C	T	rs7921647	23936387	1.30E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7921647-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	124676335	rs11248332	T	C	rs11248332	23936387	1.46E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11248332-C	Research Support, Non-U.S. Gov't	Comparative Study	T
10	124680929	rs2421162	C	A	rs2421162	23936387	1.46E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2421162-A	Research Support, Non-U.S. Gov't	Comparative Study	C
10	125681274	rs1914533	T	G	rs1914533	23936387	1.84E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1914533-G	Research Support, Non-U.S. Gov't	Comparative Study	C
10	126569993	rs7914368	C	T	rs7914368	23936387	1.94E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7914368-C	Research Support, Non-U.S. Gov't	Comparative Study	C
10	131856651	rs10829685	G	T	rs10829685	23936387	2.39E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10829685-G	Research Support, Non-U.S. Gov't	Comparative Study	G
11	2048488	rs4930144	A	G	rs4930144	23936387	7.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4930144-A	Research Support, Non-U.S. Gov't	Comparative Study	A
11	3776371	rs276892	C	T	rs276892	17558408	2.20E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NUP98
11	3796406	rs276885	G	A,C,T	rs276885	17558408	3.00E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NUP98
11	4707571	rs10836470	C	T	rs10836470	23936387	2.45E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10836470-C	Research Support, Non-U.S. Gov't	Comparative Study	C
11	8348725	rs10840025	C	T	rs10840025	23936387	1.20E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10840025-C	Research Support, Non-U.S. Gov't	Comparative Study	C
11	8369415	rs897111	G	A	rs897111	23936387	1.47E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs897111-A	Research Support, Non-U.S. Gov't	Comparative Study	A
11	17451427	rs4148621	C	A	rs4148621	23936387	1.24E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4148621-A	Research Support, Non-U.S. Gov't	Comparative Study	G
11	20275946	rs1520895	G	A	rs1520895	23936387	2.91E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1520895-A	Research Support, Non-U.S. Gov't	Comparative Study	C
11	20286574	rs7950594	G	A	rs7950594	23936387	1.72E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7950594-A	Research Support, Non-U.S. Gov't	Comparative Study	G
11	20298798	rs1108001	G	A	rs1108001	23936387	4.88E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1108001-A	Research Support, Non-U.S. Gov't	Comparative Study	T
11	21350620	rs10833507	A	G	rs10833507	23936387	1.46E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10833507-A	Research Support, Non-U.S. Gov't	Comparative Study	G
11	21357397	rs10437584	G	T	rs10437584	23936387	1.14E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10437584-G	Research Support, Non-U.S. Gov't	Comparative Study	G
11	32435529	rs2900740	G	A	rs2900740	23936387	9.60E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2900740-A	Research Support, Non-U.S. Gov't	Comparative Study	G
11	32446985	rs12293750	C	A	rs12293750	23936387	1.13E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12293750-A	Research Support, Non-U.S. Gov't	Comparative Study	C
11	34338342	rs4755368	T	C	rs4755368	23936387	2.80E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4755368-C	Research Support, Non-U.S. Gov't	Comparative Study	T
11	36470815	rs10501156	C	A	rs10501156	23936387	2.36E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10501156-A	Research Support, Non-U.S. Gov't	Comparative Study	C
11	44788115	rs10838353	A	C	rs10838353	17558408	4.80E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	TSPAN18
11	60836519	rs175131	G	A	rs175131	23936387	1.37E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs175131-A	Research Support, Non-U.S. Gov't	Comparative Study	A
11	110703667	rs226129	T	C	rs226129	23936387	9.52E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs226129-C	Research Support, Non-U.S. Gov't	Comparative Study	A
11	111196858	rs7104791	T	C	rs7104791	17558408	7.90E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	C	NA
11	111196858	rs7104791	T	C	rs7104791	22057235	1.90E-11	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
11	111668585	rs582465	C	T	rs582465	17558408	9.70E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	ALG9
11	116556865	rs1145212	G	A	rs1145212	23936387	3.00E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1145212-A	Research Support, Non-U.S. Gov't	Comparative Study	C
11	118579865	rs10892258	G	A	rs10892258	22057235	1.70E-11	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
11	118579865	rs10892258	G	A	rs10892258	23143596	1.70E-11	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
11	120544237	rs12360673	A	G	rs12360673	23936387	2.33E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12360673-A	Research Support, Non-U.S. Gov't	Comparative Study	A
11	128380974	rs11221332	C	T	rs11221332	20190752	5.00E-16	NA	1.21	[1.16-1.27]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11221332-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
11	128391937	rs61907765	C	A,G,T	rs61907765	22057235	3.40E-13	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
11	129865592	rs12793517	G	A	rs12793517	23936387	5.32E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12793517-A	Research Support, Non-U.S. Gov't	Comparative Study	G
11	131366138	rs318966	G	A	rs318966	23936387	1.17E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs318966-A	Research Support, Non-U.S. Gov't	Comparative Study	A
11	134769426	rs1478747	G	A	rs1478747	23936387	1.81E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1478747-A	Research Support, Non-U.S. Gov't	Comparative Study	C
12	332362	rs2289954	C	T	rs2289954	23936387	2.85E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2289954-C	Research Support, Non-U.S. Gov't	Comparative Study	C
12	4070800	rs624304	C	T	rs624304	23936387	2.09E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs624304-C	Research Support, Non-U.S. Gov't	Comparative Study	A
12	12521332	rs11054854	T	G	rs11054854	23936387	8.37E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11054854-G	Research Support, Non-U.S. Gov't	Comparative Study	T
12	69301287	rs2029774	T	C	rs2029774	23936387	1.09E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2029774-C	Research Support, Non-U.S. Gov't	Comparative Study	A
12	72569746	rs2730666	G	T	rs2730666	23936387	4.79E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2730666-G	Research Support, Non-U.S. Gov't	Comparative Study	G
12	75063110	rs11836636	A	G	rs11836636	23936387	2.36E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11836636-A	Research Support, Non-U.S. Gov't	Comparative Study	A
12	75077344	rs11180157	T	C	rs11180157	23936387	2.77E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11180157-C	Research Support, Non-U.S. Gov't	Comparative Study	T
12	79506862	rs17005224	G	A	rs17005224	23936387	4.65E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17005224-A	Research Support, Non-U.S. Gov't	Comparative Study	G
12	81315248	rs7487519	T	C	rs7487519	23936387	1.49E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7487519-C	Research Support, Non-U.S. Gov't	Comparative Study	C
12	86281157	rs2121889	C	T	rs2121889	23936387	8.00E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2121889-C	Research Support, Non-U.S. Gov't	Comparative Study	C
12	87640519	rs11104365	T	C	rs11104365	23936387	1.09E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11104365-C	Research Support, Non-U.S. Gov't	Comparative Study	T
12	87727594	rs3990897	C	T	rs3990897	23936387	1.22E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3990897-C	Research Support, Non-U.S. Gov't	Comparative Study	G
12	91539784	rs1803343	T	C	rs1803343	23936387	6.11E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1803343-C	Research Support, Non-U.S. Gov't	Comparative Study	A
12	106484512	rs1366041	C	T	rs1366041	23936387	2.91E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1366041-C	Research Support, Non-U.S. Gov't	Comparative Study	A
12	111884608	rs3184504	T	C	rs3184504	22057235	5.40E-21	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
12	112007756	rs653178	C	T	rs653178	18311140	8.00E-08		1.21	[1.13-1.30]	767 cases; 1,422 controls	NOPOP(2189)	ALL(2189)	NOPOP(2189)	ALL(2189)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs653178-G	Research Support, Non-U.S. Gov't	A	ATXN2
12	112007756	rs653178	C	T	rs653178	20190752	7.00E-21	NA	1.2	[1.15-1.24]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs653178-G	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	A
12	127874250	rs11059101	T	C	rs11059101	23936387	2.31E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11059101-C	Research Support, Non-U.S. Gov't	Comparative Study	T
12	132339957	rs4964933	T	C	rs4964933	23936387	9.67E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4964933-C	Research Support, Non-U.S. Gov't	Comparative Study	T
13	20912067	rs17080439	A	G	rs17080439	23936387	1.15E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17080439-A	Research Support, Non-U.S. Gov't	Comparative Study	A
13	23616490	rs2311185	A	G	rs2311185	23936387	7.81E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2311185-A	Research Support, Non-U.S. Gov't	Comparative Study	C
13	46112492	rs3014904	G	A	rs3014904	23936387	3.12E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3014904-A	Research Support, Non-U.S. Gov't	Comparative Study	A
13	50835715	rs2762051	C	T	rs2762051	20190752	7.00E-07	NA	1.13	[1.08-1.18]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2762051-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
13	72497249	rs2810134	G	A	rs2810134	23936387	7.99E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2810134-A	Research Support, Non-U.S. Gov't	Comparative Study	A
13	72497776	rs2810135	G	A	rs2810135	23936387	2.05E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2810135-A	Research Support, Non-U.S. Gov't	Comparative Study	A
13	72503504	rs1563871	C	T	rs1563871	23936387	2.99E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1563871-C	Research Support, Non-U.S. Gov't	Comparative Study	T
13	72508894	rs9542781	A	G	rs9542781	23936387	2.54E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9542781-A	Research Support, Non-U.S. Gov't	Comparative Study	A
13	73089892	rs9599966	A	G	rs9599966	23936387	2.45E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9599966-A	Research Support, Non-U.S. Gov't	Comparative Study	A
13	74934797	rs7983584	T	G	rs7983584	23936387	7.85E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7983584-G	Research Support, Non-U.S. Gov't	Comparative Study	T
13	75217454	rs2325630	T	C	rs2325630	17558408	5.50E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NA
13	85610544	rs8000505	C	T	rs8000505	23936387	1.68E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs8000505-C	Research Support, Non-U.S. Gov't	Comparative Study	T
13	106098250	rs9301029	T	C	rs9301029	23936387	3.92E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9301029-C	Research Support, Non-U.S. Gov't	Comparative Study	T
13	109037961	rs7318477	C	T	rs7318477	23936387	2.75E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7318477-C	Research Support, Non-U.S. Gov't	Comparative Study	T
14	25005585	rs987629	T	C	rs987629	23936387	8.48E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs987629-C	Research Support, Non-U.S. Gov't	Comparative Study	A
14	32384626	rs1278878	A	G	rs1278878	23936387	2.03E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1278878-A	Research Support, Non-U.S. Gov't	Comparative Study	G
14	34844376	rs1958589	T	C	rs1958589	23936387	4.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1958589-C	Research Support, Non-U.S. Gov't	Comparative Study	T
14	44519214	rs6572235	A	G	rs6572235	23936387	8.36E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6572235-A	Research Support, Non-U.S. Gov't	Comparative Study	G
14	44530722	rs1950538	C	T	rs1950538	23936387	2.09E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1950538-C	Research Support, Non-U.S. Gov't	Comparative Study	A
14	44540560	rs2415836	A	C	rs2415836	23936387	7.52E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2415836-A	Research Support, Non-U.S. Gov't	Comparative Study	C
14	61689892	rs4457900	T	G	rs4457900	23936387	2.52E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4457900-G	Research Support, Non-U.S. Gov't	Comparative Study	T
14	61692955	rs6573374	T	C	rs6573374	23936387	9.74E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6573374-C	Research Support, Non-U.S. Gov't	Comparative Study	C
14	67899267	rs4902468	C	T	rs4902468	23936387	7.06E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4902468-C	Research Support, Non-U.S. Gov't	Comparative Study	C
14	69259502	rs11851414	T	C	rs11851414	22057235	4.70E-08	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
14	69278204	rs4899260	C	T	rs4899260	20190752	4.00E-07	NA	1.12	[1.07-1.16]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4899260-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
14	77018566	rs1676235	G	A	rs1676235	23936387	2.68E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1676235-A	Research Support, Non-U.S. Gov't	Comparative Study	A
14	78781995	rs17107326	T	C	rs17107326	23936387	1.38E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17107326-C	Research Support, Non-U.S. Gov't	Comparative Study	T
14	79346136	rs2370876	A	G	rs2370876	23936387	2.94E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2370876-A	Research Support, Non-U.S. Gov't	Comparative Study	A
14	82065638	rs7159238	C	T	rs7159238	17558408	6.20E-06	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NA
14	88727027	rs724611	G	A	rs724611	23936387	7.47E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs724611-A	Research Support, Non-U.S. Gov't	Comparative Study	A
14	93550009	rs4905043	G	A	rs4905043	23936387	3.31E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4905043-A	Research Support, Non-U.S. Gov't	Comparative Study	G
14	98322480	rs1841722	G	T	rs1841722	23936387	4.85E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1841722-G	Research Support, Non-U.S. Gov't	Comparative Study	A
14	101554839	rs12147287	A	G	rs12147287	23936387	2.21E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12147287-A	Research Support, Non-U.S. Gov't	Comparative Study	A
15	22427966	rs7167893	G	A	rs7167893	23936387	2.09E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7167893-A	Research Support, Non-U.S. Gov't	Comparative Study	NA
15	23140114	rs8033142	C	T	rs8033142	23936387	1.73E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs8033142-C	Research Support, Non-U.S. Gov't	Comparative Study	T
15	25241791	rs17786183	C	T	rs17786183	23936387	1.04E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17786183-C	Research Support, Non-U.S. Gov't	Comparative Study	C
15	26336463	rs8024188	A	G	rs8024188	23936387	2.91E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs8024188-A	Research Support, Non-U.S. Gov't	Comparative Study	A
15	33528078	rs2292548	T	C	rs2292548	23936387	9.05E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2292548-C	Research Support, Non-U.S. Gov't	Comparative Study	A
15	33810168	rs6495130	G	A	rs6495130	23936387	3.72E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6495130-A	Research Support, Non-U.S. Gov't	Comparative Study	G
15	33822969	rs12900227	T	C	rs12900227	23936387	9.01E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12900227-C	Research Support, Non-U.S. Gov't	Comparative Study	T
15	33829250	rs12909478	C	T	rs12909478	23936387	3.40E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12909478-C	Research Support, Non-U.S. Gov't	Comparative Study	C
15	34953986	rs7497057	C	T	rs7497057	17558408	8.50E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NA
15	36766056	rs17703807	T	C	rs17703807	23936387	2.03E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17703807-C	Research Support, Non-U.S. Gov't	Comparative Study	C
15	52671784	rs2242058	C	T	rs2242058	23936387	2.91E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2242058-C	Research Support, Non-U.S. Gov't	Comparative Study	C
15	52687433	rs10518687	G	A	rs10518687	23936387	2.89E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10518687-A	Research Support, Non-U.S. Gov't	Comparative Study	G
15	52710340	rs10083673	G	A	rs10083673	23936387	9.62E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10083673-A	Research Support, Non-U.S. Gov't	Comparative Study	G
15	55823602	rs9806182	A	G	rs9806182	23936387	2.32E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9806182-A	Research Support, Non-U.S. Gov't	Comparative Study	A
15	75096443	rs1378938	T	C	rs1378938	22057235	7.80E-09	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
15	82206430	rs1353122	T	C	rs1353122	17558408	5.30E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NA
15	85088657	rs3883013	T	C	rs3883013	23936387	2.04E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3883013-C	Research Support, Non-U.S. Gov't	Comparative Study	A
15	85680532	rs3743157	C	A	rs3743157	23936387	1.19E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3743157-A	Research Support, Non-U.S. Gov't	Comparative Study	A
15	95609121	rs11635863	A	G	rs11635863	23936387	2.61E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11635863-A	Research Support, Non-U.S. Gov't	Comparative Study	A
16	10964118	rs6498114	G	T	rs6498114	22057235	5.80E-10	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
16	11361202	rs243323	A	G	rs243323	22057235	2.50E-05	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
16	11384956	rs9673543	A	G	rs9673543	22057235	2.00E-04	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
16	11403893	rs12928822	C	T	rs12928822	20190752	3.00E-08	NA	1.16	[1.10-1.22]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
16	12961120	rs10500391	T	G	rs10500391	17558408	8.30E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	T	NA
16	13323341	rs204034	A	G	rs204034	23936387	1.20E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs204034-A	Research Support, Non-U.S. Gov't	Comparative Study	C
16	54442483	rs8045954	A	C	rs8045954	23936387	6.55E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs8045954-A	Research Support, Non-U.S. Gov't	Comparative Study	A
16	54587432	rs16953659	A	G	rs16953659	23936387	1.82E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs16953659-A	Research Support, Non-U.S. Gov't	Comparative Study	A
16	71047484	rs195656	G	A	rs195656	23936387	7.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs195656-A	Research Support, Non-U.S. Gov't	Comparative Study	G
16	79108354	rs7194361	C	T	rs7194361	23936387	4.81E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7194361-C	Research Support, Non-U.S. Gov't	Comparative Study	C
16	81209234	rs935933	C	T	rs935933	23936387	2.10E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs935933-C	Research Support, Non-U.S. Gov't	Comparative Study	T
17	18901	rs8064924	G	A	rs8064924	23936387	1.84E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs8064924-A	Research Support, Non-U.S. Gov't	Comparative Study	A
17	6023338	rs4254372	G	A	rs4254372	23936387	1.35E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4254372-A	Research Support, Non-U.S. Gov't	Comparative Study	A
17	12736766	rs12600697	C	T	rs12600697	23936387	4.24E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12600697-C	Research Support, Non-U.S. Gov't	Comparative Study	C
17	19969397	rs7209752	A	G	rs7209752	23936387	1.06E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7209752-A	Research Support, Non-U.S. Gov't	Comparative Study	G
17	35731081	rs8081319	A	G	rs8081319	24999842	8.00E-07	NA	1.36	[1.20-1.54]	1,550 European ancestry cases; 3,084 European ancestry controls	European(4634)	ALL(4634)	EUR(4634)	ALL(4634)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	G	ACACA
17	44865439	rs2074404	T	G	rs2074404	20190752	1.00E-06	NA	1.11	[1.06-1.16]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
17	54611291	rs17760268	C	T	rs17760268	23936387	4.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17760268-C	Research Support, Non-U.S. Gov't	Comparative Study	C
17	72065264	rs9906003	G	A	rs9906003	23936387	5.53E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9906003-A	Research Support, Non-U.S. Gov't	Comparative Study	G
17	72074718	rs12942418	G	A	rs12942418	23936387	5.71E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12942418-A	Research Support, Non-U.S. Gov't	Comparative Study	G
17	72503355	rs1171208	G	A	rs1171208	23936387	1.03E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1171208-A	Research Support, Non-U.S. Gov't	Comparative Study	T
17	72508425	rs1107704	A	G	rs1107704	23936387	2.54E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1107704-A	Research Support, Non-U.S. Gov't	Comparative Study	G
17	77400623	rs11656673	C	T	rs11656673	23936387	2.68E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11656673-C	Research Support, Non-U.S. Gov't	Comparative Study	C
17	78297779	rs7225029	G	A	rs7225029	23936387	6.74E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7225029-A	Research Support, Non-U.S. Gov't	Comparative Study	G
18	5753004	rs1917917	C	T	rs1917917	23936387	1.37E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1917917-C	Research Support, Non-U.S. Gov't	Comparative Study	T
18	6092906	rs7245021	T	C	rs7245021	23936387	1.85E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7245021-C	Research Support, Non-U.S. Gov't	Comparative Study	C
18	11074577	rs17106	C	T	rs17106	23936387	2.08E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17106-C	Research Support, Non-U.S. Gov't	Comparative Study	C
18	12809340	rs1893217	A	G	rs1893217	20190752	3.00E-10	NA	1.17	[1.12-1.23]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1893217-G	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
18	12843137	rs11875687	T	C	rs11875687	22057235	1.90E-10	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
18	12843137	rs11875687	T	C	rs11875687	23143596	1.90E-10	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
18	12857758	rs62097857	G	A	rs62097857	22057235	5.20E-05	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
18	12857758	rs62097857	G	A	rs62097857	23143596	0.000052	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
18	40183618	rs2878722	G	A	rs2878722	23936387	7.51E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2878722-A	Research Support, Non-U.S. Gov't	Comparative Study	A
18	42152467	rs4467169	A	G	rs4467169	23936387	2.67E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4467169-A	Research Support, Non-U.S. Gov't	Comparative Study	A
18	42155773	rs10164078	G	A	rs10164078	23936387	1.59E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10164078-A	Research Support, Non-U.S. Gov't	Comparative Study	G
18	56202768	rs3809983	C	A	rs3809983	17558408	3.70E-06	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	ALPK2
18	56203074	rs3809982	G	A	rs3809982	17558408	7.00E-06	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	C	ALPK2
18	56204932	rs3809973	T	G	rs3809973	17558408	6.60E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	ALPK2
18	56204991	rs3809970	C	T	rs3809970	17558408	9.20E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	ALPK2
18	56205262	rs12103986	A	C,G	rs12103986	17558408	7.80E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	C	ALPK2
18	60857160	rs17679032	T	C	rs17679032	23936387	6.58E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17679032-C	Research Support, Non-U.S. Gov't	Comparative Study	T
18	66883372	rs583991	C	T	rs583991	23936387	1.63E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs583991-C	Research Support, Non-U.S. Gov't	Comparative Study	G
18	67365668	rs4426448	A	G	rs4426448	23936387	2.81E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4426448-A	Research Support, Non-U.S. Gov't	Comparative Study	G
18	70744164	rs2194633	A	G	rs2194633	23936387	1.31E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2194633-A	Research Support, Non-U.S. Gov't	Comparative Study	A
18	76137272	rs7245277	T	C	rs7245277	17558408	1.90E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	C	NA
19	638853	rs3814892	G	A	rs3814892	23936387	2.08E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3814892-A	Research Support, Non-U.S. Gov't	Comparative Study	C
19	1697633	rs9676750	A	G	rs9676750	23936387	1.39E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9676750-A	Research Support, Non-U.S. Gov't	Comparative Study	G
19	3565909	rs6510761	T	C	rs6510761	23936387	5.65E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6510761-C	Research Support, Non-U.S. Gov't	Comparative Study	T
19	8566880	rs10403336	C	T	rs10403336	23936387	5.79E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10403336-C	Research Support, Non-U.S. Gov't	Comparative Study	C
19	13467036	rs12985786	G	A	rs12985786	23936387	1.68E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs12985786-A	Research Support, Non-U.S. Gov't	Comparative Study	G
19	29980510	rs1036229	G	A	rs1036229	17558408	2.50E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	LOC284395
19	32979847	rs11671562	C	T	rs11671562	23936387	2.64E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11671562-C	Research Support, Non-U.S. Gov't	Comparative Study	C
19	45134110	rs846866	A	C	rs846866	23936387	2.97E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs846866-A	Research Support, Non-U.S. Gov't	Comparative Study	C
19	45146103	rs7255066	T	C	rs7255066	23936387	2.10E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7255066-C	Research Support, Non-U.S. Gov't	Comparative Study	C
19	51377163	rs2664156	T	C	rs2664156	23936387	6.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2664156-C	Research Support, Non-U.S. Gov't	Comparative Study	C,T
20	2315305	rs13037722	T	C	rs13037722	23936387	2.31E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs13037722-C	Research Support, Non-U.S. Gov't	Comparative Study	T
20	4443634	rs297676	G	A	rs297676	23936387	2.01E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs297676-A	Research Support, Non-U.S. Gov't	Comparative Study	A
20	6086772	rs6053908	C	T	rs6053908	17558408	5.10E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	C	FERMT1
20	6893128	rs6038644	A	G	rs6038644	23936387	1.09E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6038644-A	Research Support, Non-U.S. Gov't	Comparative Study	G
20	15602333	rs200755	G	A	rs200755	17558408	7.90E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	A	MACROD2
20	23801747	rs6076132	A	C	rs6076132	23936387	6.74E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6076132-A	Research Support, Non-U.S. Gov't	Comparative Study	A
20	44968255	rs6065961	C	A	rs6065961	23936387	2.98E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6065961-A	Research Support, Non-U.S. Gov't	Comparative Study	C
20	50647891	rs17803622	C	T	rs17803622	23936387	2.28E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17803622-C	Research Support, Non-U.S. Gov't	Comparative Study	C
20	53414539	rs157640	T	G	rs157640	23936387	5.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs157640-G	Research Support, Non-U.S. Gov't	Comparative Study	T
20	53420586	rs157649	G	A	rs157649	23936387	6.33E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs157649-A	Research Support, Non-U.S. Gov't	Comparative Study	A
21	10971951	rs10439884	G	A	rs10439884	23936387	2.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs10439884-A	Research Support, Non-U.S. Gov't	Comparative Study	G
21	17832871	rs990628	G	A	rs990628	23936387	5.10E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs990628-A	Research Support, Non-U.S. Gov't	Comparative Study	A
21	43458706	rs4920059	C	T	rs4920059	23936387	2.79E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4920059-C	Research Support, Non-U.S. Gov't	Comparative Study	C
21	43855067	rs1893592	A	C	rs1893592	22057235	3.00E-09	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
21	45629121	rs58911644	A	T	rs58911644	22057235	6.20E-07	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
21	45647421	rs4819388	T	C	rs4819388	20190752	2.00E-09	NA	1.14	[1.09-1.19]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
22	16504399	rs4911642	C	T	rs4911642	23936387	5.00E-06	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4911642-C	Research Support, Non-U.S. Gov't	Comparative Study	T
22	18077720	rs1296820	G	T	rs1296820	23936387	8.68E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1296820-G	Research Support, Non-U.S. Gov't	Comparative Study	G
22	18079518	rs1296826	T	C	rs1296826	23936387	6.11E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1296826-C	Research Support, Non-U.S. Gov't	Comparative Study	C
22	18226764	rs8190315	T	C	rs8190315	23936387	2.12E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs8190315-C	Research Support, Non-U.S. Gov't	Comparative Study	A
22	18261496	rs5992834	G	A	rs5992834	23936387	2.56E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs5992834-A	Research Support, Non-U.S. Gov't	Comparative Study	A
22	18395877	rs5747405	C	T	rs5747405	23936387	1.87E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs5747405-C	Research Support, Non-U.S. Gov't	Comparative Study	C
22	18504801	rs390495	T	G	rs390495	23936387	1.34E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs390495-G	Research Support, Non-U.S. Gov't	Comparative Study	G
22	21462353	rs140392	A	G	rs140392	23936387	4.53E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs140392-A	Research Support, Non-U.S. Gov't	Comparative Study	G
22	21979289	rs4821124	T	C	rs4821124	22057235	5.70E-11	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
22	21982892	rs2298428	C	T	rs2298428	20190752	2.00E-07	NA	1.13	[1.08-1.19]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2298428-A	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	C
22	23031579	rs6003222	T	C	rs6003222	23936387	1.27E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6003222-C	Research Support, Non-U.S. Gov't	Comparative Study	T
22	23035233	rs3814997	T	C	rs3814997	23936387	1.23E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3814997-C	Research Support, Non-U.S. Gov't	Comparative Study	NA
22	24257779	rs9608216	C	T	rs9608216	23936387	1.70E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9608216-C	Research Support, Non-U.S. Gov't	Comparative Study	C
22	25668730	rs5996879	C	A	rs5996879	23936387	1.03E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs5996879-A	Research Support, Non-U.S. Gov't	Comparative Study	C
22	26884039	rs4820682	G	A	rs4820682	23936387	2.92E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4820682-A	Research Support, Non-U.S. Gov't	Comparative Study	G
22	26894985	rs2187956	C	T	rs2187956	23936387	2.87E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2187956-C	Research Support, Non-U.S. Gov't	Comparative Study	C
22	26895337	rs1008530	G	A	rs1008530	23936387	2.87E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs1008530-A	Research Support, Non-U.S. Gov't	Comparative Study	G
22	39661597	rs17304019	G	A	rs17304019	23936387	2.55E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs17304019-A	Research Support, Non-U.S. Gov't	Comparative Study	G
22	44708655	rs7510924	T	C	rs7510924	23936387	1.05E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7510924-C	Research Support, Non-U.S. Gov't	Comparative Study	C
22	46570342	rs9626737	A	G	rs9626737	23936387	1.88E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs9626737-A	Research Support, Non-U.S. Gov't	Comparative Study	A
X	12971524	rs5979785	C	T	rs5979785	20190752	6.00E-08	NA	1.14	[1.09-1.19]	4,533 European descent cases; 10,750 European descent controls	European(15283)	ALL(15283)	EUR(15283)	ALL(15283)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	T
X	51610969	rs5991739	G	A	rs5991739	23936387	2.97E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs5991739-A	Research Support, Non-U.S. Gov't	Comparative Study	A
X	55361937	rs11091412	C	T	rs11091412	23936387	8.99E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11091412-T	Research Support, Non-U.S. Gov't	Comparative Study	T
X	64087388	rs5918890	C	T	rs5918890	23936387	3.47E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs5918890-A	Research Support, Non-U.S. Gov't	Comparative Study	C
X	67358208	rs5919529	T	C	rs5919529	23936387	9.45E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs5919529-A	Research Support, Non-U.S. Gov't	Comparative Study	T
X	88685058	rs2534116	C	T	rs2534116	23936387	2.67E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2534116-T	Research Support, Non-U.S. Gov't	Comparative Study	C
X	92119963	rs35766825	A	G	rs35766825	23936387	1.94E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs35766825-G	Research Support, Non-U.S. Gov't	Comparative Study	A
X	93323025	rs5983336	A	C	rs5983336	23936387	8.58E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs5983336-C	Research Support, Non-U.S. Gov't	Comparative Study	C
X	100525968	rs11092298	T	C	rs11092298	23936387	2.84E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11092298-C	Research Support, Non-U.S. Gov't	Comparative Study	T
X	100532924	rs3788765	A	G	rs3788765	23936387	2.84E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs3788765-G	Research Support, Non-U.S. Gov't	Comparative Study	T
X	113820986	rs543229	A	G	rs543229	23936387	6.74E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs543229-C	Research Support, Non-U.S. Gov't	Comparative Study	C
X	113934856	rs5988087	C	T	rs5988087	23936387	3.93E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs5988087-A	Research Support, Non-U.S. Gov't	Comparative Study	C
X	113944060	rs11167436	C	A	rs11167436	23936387	6.47E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs11167436-A	Research Support, Non-U.S. Gov't	Comparative Study	A
X	114047867	rs4332303	T	C	rs4332303	23936387	3.93E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs4332303-A	Research Support, Non-U.S. Gov't	Comparative Study	C
X	114263036	rs7891628	A	C	rs7891628	23936387	3.47E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs7891628-C	Research Support, Non-U.S. Gov't	Comparative Study	A
X	122944839	rs3124045	G	A	rs3124045	17558408	2.90E-05	NA	NA	NA	778 cases; 1,422 controls	NOPOP(2200)	ALL(2200)	NOPOP(2200)	ALL(2200)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, Non-U.S. Gov't	G	NA
X	152809742	rs6643623	T	C	rs6643623	23936387	9.11E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs6643623-G	Research Support, Non-U.S. Gov't	Comparative Study	C
X	153248248	rs13397	G	A	rs13397	22057235	2.70E-08	Celiac disease	NA	NA	12041 European ancestry cases; 12228 controls	NOPOP(12228)	European(12041)	ALL(24269)	NOPOP(12228)	EUR(12041)	ALL(24269)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural
X	153248248	rs13397	G	A	rs13397	23143596	0.000000027	NA	NA	NA	11475 European ancestry cases; 15870 European ancestry controls	European(27345)	ALL(27345)	EUR(27345)	ALL(27345)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	G
Y	4935714	rs2571653	C	A	rs35842692	23936387	7.48E-05	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs35842692-C	Research Support, Non-U.S. Gov't	Comparative Study	G
Y	5411068	rs2578787	A	G	rs35361563	23936387	1.68E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs35361563-A	Research Support, Non-U.S. Gov't	Comparative Study	NA
Y	5608402	rs2556916	A	C	rs2556916	23936387	1.47E-04	NA	NA	NA	206 European ancestry trios	European(206)	ALL(206)	EUR(206)	ALL(206)	Celiac disease	HPOID:0001438	Abnormality of the abdomen	DOID:10608	celiac disease	D002446	Celiac Disease	EFOID:0001060	celiac disease	Celiac disease	rs2556916-A	Research Support, Non-U.S. Gov't	Comparative Study	NA

Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
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Chemical(Total Drugs:0)
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FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
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