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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   renal cell carcinoma
  

Disease ID 98
Disease renal cell carcinoma
Definition
A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma.
Synonym
adenocarcinoma cells renal
adenocarcinoma kidneys
adenocarcinoma of kidney
adenocarcinoma of the kidney
adenocarcinoma renal
adenocarcinoma, renal
adenocarcinoma, renal cell
adenocarcinomas, renal cell
cancer cell renal
cancer cells renal
cancer, renal cell
cancers, renal cell
carcinoma cell renal
carcinoma cells renal
carcinoma kidney
carcinoma of kidney
carcinoma renal
carcinoma, nephroid
carcinoma, renal cell
carcinoma, renal cell [disease/finding]
carcinoma, renal cell, malignant
carcinomas renal
carcinomas, nephroid
carcinomas, renal cell
cell renal cancer
grawitz tumor
hypernephroid carcinomas
hypernephroma
kidney (renal cell) cancer
kidney adenocarcinoma
kidney cancer, renal cell adenocarcinoma
kidney carcinoma
nephroid carcinoma
nephroid carcinomas
of kidney carcinoma
rcc
rccs
renal adenocarcinoma
renal cancer, adenocarcinoma
renal carcinoma
renal cell adenocarcinoma
renal cell adenocarcinomas
renal cell cancer
renal cell cancers
renal cell carcinoma (disorder)
renal cell carcinoma (morphologic abnormality)
renal cell carcinoma - morphology
renal cell carcinoma, nos
renal cell carcinoma, papillary
renal cell carcinoma, stage unspecified
renal cell carcinomas
Orphanet
OMIM
DOID
UMLS
C0007134
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:180)
C0040053  |  thrombus  |  55
C0040053  |  thrombosis  |  12
C0019562  |  lindau disease  |  11
C0028754  |  obesity  |  11
C0022658  |  renal disease  |  11
C0020538  |  hypertension  |  11
C0022661  |  end-stage renal disease  |  10
C0022658  |  kidney disease  |  8
C0019562  |  von hippel-lindau disease  |  7
C0153676  |  lung metastases  |  7
C0019562  |  hippel-lindau disease  |  7
C0022661  |  chronic kidney disease  |  7
C0032285  |  pneumonitis  |  6
C0220650  |  brain metastases  |  6
C0007134  |  renal cell carcinoma  |  5
C0346010  |  birt-hogg-dube syndrome  |  5
C0153676  |  lung metastasis  |  5
C0153676  |  pulmonary metastasis  |  5
C0220650  |  brain metastasis  |  5
C0018801  |  heart failure  |  4
C0024623  |  gastric cancer  |  4
C0153676  |  pulmonary metastases  |  4
C0041341  |  tuberous sclerosis  |  4
C0025202  |  melanoma  |  4
C0008325  |  cholecystitis  |  4
C0011847  |  diabetes  |  4
C0024299  |  lymphoma  |  3
C0029463  |  osteosarcoma  |  3
C0020676  |  hypothyroidism  |  3
C0494165  |  liver metastases  |  3
C0011849  |  diabetes mellitus  |  3
C0019562  |  von hippel lindau disease  |  3
C0836924  |  thrombocytosis  |  3
C0023827  |  liposarcoma  |  3
C0036202  |  sarcoid  |  3
C1306837  |  papillary renal cell carcinoma  |  3
C0267841  |  acalculous cholecystitis  |  3
C0740457  |  renal cancer  |  3
C0278678  |  metastatic renal cell carcinoma  |  3
C0042384  |  vasculitis  |  2
C0085652  |  pyoderma gangrenosum  |  2
C0022679  |  cystic kidney  |  2
C0206654  |  leiomyomatosis  |  2
C0206734  |  hemangioblastoma  |  2
C0740457  |  kidney cancer  |  2
C0007138  |  urothelial carcinoma  |  2
C0751571  |  urological cancers  |  2
C0085413  |  autosomal dominant polycystic kidney  |  2
C0020437  |  hypercalcemia  |  2
C0007134  |  renal carcinoma  |  2
C0036202  |  sarcoidosis  |  2
C0686619  |  lymph node metastases  |  2
C0002871  |  anemia  |  2
C0206633  |  angiomyolipoma  |  2
C0948265  |  metabolic syndrome  |  2
C0442874  |  neuropathy  |  2
C0085413  |  autosomal dominant polycystic kidney disease  |  2
C0494165  |  hepatic metastases  |  2
C0034150  |  purpura  |  2
C0279702  |  clear cell renal cell carcinoma  |  2
C0751571  |  urological cancer  |  2
C0241961  |  renal angiomyolipoma  |  2
C0023903  |  liver tumor  |  1
C0041341  |  tuberous sclerosis complex  |  1
C0699790  |  colon carcinoma  |  1
C0020428  |  aldosteronism  |  1
C0153687  |  skin metastasis  |  1
C0020538  |  high blood pressure  |  1
C0007115  |  thyroid ca  |  1
C0018916  |  hemangioma  |  1
C0018552  |  hamartomas  |  1
C0023267  |  leiomyomas  |  1
C0007133  |  papillary carcinoma  |  1
C0027708  |  wilms tumor  |  1
C0027708  |  nephroblastoma  |  1
C0021933  |  intussusception  |  1
C0001173  |  gastric outlet obstruction  |  1
C0035328  |  retinal vein occlusion  |  1
C0376545  |  hematological malignancies  |  1
C0034212  |  pyoderma  |  1
C0278883  |  metastatic melanoma  |  1
C0025202  |  melanomas  |  1
C0235974  |  pancreatic cancer  |  1
C0032000  |  pituitary adenomas  |  1
C0003864  |  arthritis  |  1
C0494165  |  liver metastasis  |  1
C0151436  |  leukocytoclastic vasculitis  |  1
C0549473  |  thyroid carcinoma  |  1
C0043117  |  idiopathic thrombocytopenic purpura  |  1
C0270922  |  demyelinating neuropathy  |  1
C0019618  |  histiocytosis  |  1
C0751690  |  malignant peripheral nerve sheath tumor  |  1
C1691228  |  renal cystic disease  |  1
C0021831  |  bowel disease  |  1
C0027726  |  nephrotic syndrome  |  1
C0030805  |  bullous pemphigoid  |  1
C0206681  |  clear cell adenocarcinoma  |  1
C0022661  |  chronic renal failure  |  1
C0001627  |  congenital adrenal hyperplasia  |  1
C0007137  |  squamous cell carcinoma  |  1
C0014859  |  esophageal cancer  |  1
C0008370  |  cholestasis  |  1
C0001430  |  adenoma  |  1
C0032000  |  pituitary adenoma  |  1
C0021053  |  immune disease  |  1
C0003873  |  rheumatoid arthritis  |  1
C1565489  |  renal insufficiency  |  1
C0023530  |  leukopenia  |  1
C0029132  |  optic neuropathy  |  1
C1384514  |  primary aldosteronism  |  1
C0020502  |  hyperparathyroidism  |  1
C0035078  |  renal failure  |  1
C0155773  |  portal vein thrombosis  |  1
C0007137  |  squamous cell carcinomas  |  1
C0235974  |  carcinoma of the pancreas  |  1
C0042214  |  vaccinia  |  1
C0043117  |  immune thrombocytopenic purpura  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0010481  |  cushing's syndrome  |  1
C0334684  |  renal adenoma  |  1
C0007642  |  cellulitis  |  1
C0206667  |  adrenal adenoma  |  1
C0025202  |  malignant melanoma  |  1
C0023267  |  leiomyoma  |  1
C0023434  |  chronic lymphocytic leukaemia  |  1
C0002895  |  sickle cell disease  |  1
C0242231  |  coronary artery stenosis  |  1
C0024236  |  lymphedema  |  1
C0014868  |  esophagitis  |  1
C0004030  |  aspergillosis  |  1
C0019829  |  hodgkin lymphoma  |  1
C0022660  |  acute kidney failure  |  1
C0854178  |  adrenal metastases  |  1
C0019562  |  von hippel-lindau syndrome  |  1
C0022661  |  chronic renal disease  |  1
C0037054  |  sickle-cell trait  |  1
C0030421  |  paraganglioma  |  1
C0035078  |  kidney failure  |  1
C0005684  |  bladder cancer  |  1
C0019204  |  hepatocellular carcinoma  |  1
C0009402  |  colorectal carcinoma  |  1
C0023448  |  lymphocytic leukaemia  |  1
C0017525  |  giant cell tumors  |  1
C0007114  |  skin cancer  |  1
C1621895  |  adrenal hyperplasia  |  1
C0346976  |  pancreatic metastasis  |  1
C0149925  |  small cell carcinoma  |  1
C0024305  |  non-hodgkin lymphoma  |  1
C1266045  |  metanephric adenoma  |  1
C0021390  |  inflammatory bowel disease  |  1
C0006142  |  breast cancer  |  1
C0002871  |  anaemia  |  1
C0151436  |  cutaneous leukocytoclastic vasculitis  |  1
C0221002  |  primary hyperparathyroidism  |  1
C1561644  |  chronic kidney disease (ckd)  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0033117  |  priapism  |  1
C0018552  |  hamartoma  |  1
C0007113  |  rectal carcinoma  |  1
C0346255  |  renal oncocytoma  |  1
C0019621  |  langerhans cell histiocytosis  |  1
C0034065  |  pulmonary embolism  |  1
C0018802  |  congestive heart failure  |  1
C0007112  |  prostatic adenocarcinoma  |  1
C0017525  |  giant cell tumor  |  1
C0023801  |  lipomatosis  |  1
C0271355  |  sixth nerve palsy  |  1
C0020459  |  hyperinsulinism  |  1
C0221348  |  yellow nail syndrome  |  1
C0034931  |  reflex sympathetic dystrophy  |  1
C0022354  |  cholestatic jaundice  |  1
C1266042  |  chromophobe renal cell carcinoma  |  1
C0154841  |  central retinal vein occlusion  |  1
C0022116  |  ischemia  |  1
C0024143  |  lupus nephritis  |  1
C0032285  |  pneumonia  |  1
C0027708  |  nephroma  |  1
C0030805  |  pemphigoid  |  1
C0001815  |  myelofibrosis  |  1
C0026896  |  myasthenia gravis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:125)
216  |  ALDH1A1  |  CTD_human
4286  |  MITF  |  CTD_human
8743  |  TNFSF10  |  CTD_human
3329  |  HSPD1  |  CTD_human
11236  |  RNF139  |  CTD_human
5970  |  RELA  |  CTD_human
1938  |  EEF2  |  CTD_human
2952  |  GSTT1  |  CTD_human
3945  |  LDHB  |  CTD_human
7248  |  TSC1  |  CTD_human
8314  |  BAP1  |  CTD_human
5443  |  POMC  |  CTD_human
5728  |  PTEN  |  CTD_human
3315  |  HSPB1  |  CTD_human
144132  |  DNHD1  |  CTD_human
3440  |  IFNA2  |  CTD_human
25844  |  YIPF3  |  CTD_human
158584  |  FAAH2  |  CTD_human
332  |  BIRC5  |  CTD_human
7157  |  TP53  |  CTD_human
5816  |  PVALB  |  CTD_human
9839  |  ZEB2  |  GWASCAT
3569  |  IL6  |  CTD_human
4233  |  MET  |  CLINVAR;CTD_human
210  |  ALAD  |  CTD_human
9745  |  ZNF536  |  CTD_human
3897  |  L1CAM  |  CTD_human
5230  |  PGK1  |  CTD_human
9817  |  KEAP1  |  CTD_human
29072  |  SETD2  |  CTD_human
6261  |  RYR1  |  CTD_human
10397  |  NDRG1  |  CTD_human
1509  |  CTSD  |  CTD_human
201163  |  FLCN  |  CTD_human
23224  |  SYNE2  |  CTD_human
590  |  BCHE  |  CTD_human
6928  |  HNF1B  |  CTD_human
2034  |  EPAS1  |  CTD_human;GWASCAT
6648  |  SOD2  |  CTD_human
8738  |  CRADD  |  CTD_human
54790  |  TET2  |  CTD_human
10950  |  BTG3  |  CTD_human
4968  |  OGG1  |  CTD_human
7052  |  TGM2  |  CTD_human
3035  |  HARS  |  CTD_human
6513  |  SLC2A1  |  CTD_human
2944  |  GSTM1  |  CTD_human
5290  |  PIK3CA  |  CTD_human
1612  |  DAPK1  |  CTD_human
2950  |  GSTP1  |  CTD_human
5743  |  PTGS2  |  CTD_human
2064  |  ERBB2  |  CTD_human
23042  |  PDXDC1  |  CTD_human
238  |  ALK  |  CTD_human
6927  |  HNF1A  |  CTD_human
374393  |  FAM111B  |  CTD_human
23532  |  PRAME  |  CTD_human
1410  |  CRYAB  |  CTD_human
91662  |  NLRP12  |  CTD_human
3570  |  IL6R  |  CTD_human
79026  |  AHNAK  |  CTD_human
4771  |  NF2  |  CTD_human
84433  |  CARD11  |  CTD_human
7428  |  VHL  |  CTD_human
307  |  ANXA4  |  CTD_human
8407  |  TAGLN2  |  CTD_human
5546  |  PRCC  |  CTD_human
3313  |  HSPA9  |  CTD_human
81562  |  LMAN2L  |  CTD_human
353  |  APRT  |  CTD_human
55193  |  PBRM1  |  CTD_human
8028  |  MLLT10  |  CTD_human
56776  |  FMN2  |  CTD_human
55367  |  PIDD1  |  CTD_human
43  |  ACHE  |  CTD_human
4585  |  MUC4  |  CTD_human
8790  |  FPGT  |  CTD_human
50944  |  SHANK1  |  CTD_human
2475  |  MTOR  |  CTD_human
3778  |  KCNMA1  |  CTD_human
3596  |  IL13  |  CTD_human
5058  |  PAK1  |  CTD_human
89795  |  NAV3  |  CTD_human
5162  |  PDHB  |  CTD_human
8242  |  KDM5C  |  CTD_human
9820  |  CUL7  |  CTD_human
91752  |  ZNF804A  |  CTD_human
3855  |  KRT7  |  CTD_human
95  |  ACY1  |  CTD_human
25953  |  PNKD  |  CTD_human
23037  |  PDZD2  |  GWASCAT
1381  |  CRABP1  |  CTD_human
10404  |  CPQ  |  CTD_human
6526  |  SLC5A3  |  CTD_human
283092  |  OR4C13  |  CTD_human
2705  |  GJB1  |  CTD_human
8633  |  UNC5C  |  CTD_human
91661  |  ZNF765  |  CTD_human
2321  |  FLT1  |  CTD_human
317  |  APAF1  |  CTD_human
343930  |  MSGN1  |  CTD_human
835  |  CASP2  |  CTD_human
1508  |  CTSB  |  CTD_human
9045  |  RPL14  |  CTD_human
949  |  SCARB1  |  CTD_human;GWASCAT
57731  |  SPTBN4  |  CTD_human
2886  |  GRB7  |  CTD_human
79444  |  BIRC7  |  CTD_human
7030  |  TFE3  |  CTD_human
53353  |  LRP1B  |  CTD_human
84925  |  DIRC2  |  CTD_human
3856  |  KRT8  |  CTD_human
822  |  CAPG  |  CTD_human
4074  |  M6PR  |  CTD_human
5037  |  PEBP1  |  CTD_human
3882  |  KRT32  |  CTD_human
120892  |  LRRK2  |  CTD_human
284013  |  VMO1  |  CTD_human
55745  |  AP5M1  |  CTD_human
3566  |  IL4R  |  CTD_human
1265  |  CNN2  |  CTD_human
11214  |  AKAP13  |  CTD_human
114788  |  CSMD3  |  CTD_human
6423  |  SFRP2  |  CTD_human
142685  |  ASB15  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:129)
2034  |  EPAS1  |  CIPHER;CTD_human
390218  |  IFITM9P  |  CIPHER
949  |  SCARB1  |  CIPHER;CTD_human
8082  |  SSPN  |  CIPHER
3105  |  HLA-A  |  CIPHER
6390  |  SDHB  |  CIPHER
7421  |  VDR  |  CIPHER
7428  |  VHL  |  CIPHER;CTD_human
8743  |  TNFSF10  |  CTD_human
11236  |  RNF139  |  CTD_human
144132  |  DNHD1  |  CTD_human
25844  |  YIPF3  |  CTD_human
158584  |  FAAH2  |  CTD_human
5816  |  PVALB  |  CTD_human
4233  |  MET  |  CTD_human
2952  |  GSTT1  |  CTD_human
5230  |  PGK1  |  CTD_human
9817  |  KEAP1  |  CTD_human
23224  |  SYNE2  |  CTD_human
4968  |  OGG1  |  CTD_human
3315  |  HSPB1  |  CTD_human
2944  |  GSTM1  |  CTD_human
7052  |  TGM2  |  CTD_human
3329  |  HSPD1  |  CTD_human
23042  |  PDXDC1  |  CTD_human
5743  |  PTGS2  |  CTD_human
1938  |  EEF2  |  CTD_human
79026  |  AHNAK  |  CTD_human
6921  |  TCEB1  |  CTD_human
8407  |  TAGLN2  |  CTD_human
3569  |  IL6  |  CTD_human
5546  |  PRCC  |  CTD_human
81562  |  LMAN2L  |  CTD_human
56776  |  FMN2  |  CTD_human
55367  |  PIDD1  |  CTD_human
43  |  ACHE  |  CTD_human
4585  |  MUC4  |  CTD_human
8790  |  FPGT  |  CTD_human
201163  |  FLCN  |  CTD_human
23532  |  PRAME  |  CTD_human
7248  |  TSC1  |  CTD_human
50944  |  SHANK1  |  CTD_human
3596  |  IL13  |  CTD_human
1509  |  CTSD  |  CTD_human
5058  |  PAK1  |  CTD_human
89795  |  NAV3  |  CTD_human
84433  |  CARD11  |  CTD_human
9820  |  CUL7  |  CTD_human
210  |  ALAD  |  CTD_human
95  |  ACY1  |  CTD_human
10404  |  CPQ  |  CTD_human
6526  |  SLC5A3  |  CTD_human
283092  |  OR4C13  |  CTD_human
307  |  ANXA4  |  CTD_human
8633  |  UNC5C  |  CTD_human
25953  |  PNKD  |  CTD_human
91661  |  ZNF765  |  CTD_human
2475  |  MTOR  |  CTD_human
91662  |  NLRP12  |  CTD_human
9745  |  ZNF536  |  CTD_human
374393  |  FAM111B  |  CTD_human
10950  |  BTG3  |  CTD_human
2950  |  GSTP1  |  CTD_human
5162  |  PDHB  |  CTD_human
343930  |  MSGN1  |  CTD_human
5290  |  PIK3CA  |  CTD_human
835  |  CASP2  |  CTD_human
1410  |  CRYAB  |  CTD_human
3313  |  HSPA9  |  CTD_human
9045  |  RPL14  |  CTD_human
54790  |  TET2  |  CTD_human
2886  |  GRB7  |  CTD_human
8314  |  BAP1  |  CTD_human
79444  |  BIRC7  |  CTD_human
332  |  BIRC5  |  CTD_human
6928  |  HNF1B  |  CTD_human
6927  |  HNF1A  |  CTD_human
3945  |  LDHB  |  CTD_human
53353  |  LRP1B  |  CTD_human
3035  |  HARS  |  CTD_human
590  |  BCHE  |  CTD_human
84925  |  DIRC2  |  CTD_human
238  |  ALK  |  CTD_human
216  |  ALDH1A1  |  CTD_human
4771  |  NF2  |  CTD_human
3856  |  KRT8  |  CTD_human
3855  |  KRT7  |  CTD_human
91752  |  ZNF804A  |  CTD_human
7157  |  TP53  |  CTD_human
8738  |  CRADD  |  CTD_human
1381  |  CRABP1  |  CTD_human
3897  |  L1CAM  |  CTD_human
57731  |  SPTBN4  |  CTD_human
3440  |  IFNA2  |  CTD_human
4074  |  M6PR  |  CTD_human
5037  |  PEBP1  |  CTD_human
1508  |  CTSB  |  CTD_human
353  |  APRT  |  CTD_human
55193  |  PBRM1  |  CTD_human
29072  |  SETD2  |  CTD_human
822  |  CAPG  |  CTD_human
3882  |  KRT32  |  CTD_human
120892  |  LRRK2  |  CTD_human
5443  |  POMC  |  CTD_human
1612  |  DAPK1  |  CTD_human
284013  |  VMO1  |  CTD_human
8242  |  KDM5C  |  CTD_human
55745  |  AP5M1  |  CTD_human
3570  |  IL6R  |  CTD_human
3566  |  IL4R  |  CTD_human
2064  |  ERBB2  |  CTD_human
6261  |  RYR1  |  CTD_human
5728  |  PTEN  |  CTD_human
317  |  APAF1  |  CTD_human
6513  |  SLC2A1  |  CTD_human
2321  |  FLT1  |  CTD_human
1265  |  CNN2  |  CTD_human
2705  |  GJB1  |  CTD_human
5970  |  RELA  |  CTD_human
11214  |  AKAP13  |  CTD_human
6648  |  SOD2  |  CTD_human
3778  |  KCNMA1  |  CTD_human
114788  |  CSMD3  |  CTD_human
7030  |  TFE3  |  CTD_human
10397  |  NDRG1  |  CTD_human
8028  |  MLLT10  |  CTD_human
4286  |  MITF  |  CTD_human
6423  |  SFRP2  |  CTD_human
142685  |  ASB15  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:867)
154664  |  ABCA13  |  1.061  |  DISEASES
154664  |  ABCA13  |  1.023  |  DISEASES
641372  |  ACOT6  |  1.947  |  DISEASES
641372  |  ACOT6  |  1.909  |  DISEASES
60  |  ACTB  |  1.582  |  DISEASES
60  |  ACTB  |  1.515  |  DISEASES
81569  |  ACTL8  |  1.182  |  DISEASES
81569  |  ACTL8  |  1.144  |  DISEASES
95  |  ACY1  |  2.701  |  DISEASES
95  |  ACY1  |  2.663  |  DISEASES
174  |  AFP  |  2.134  |  DISEASES
174  |  AFP  |  2.063  |  DISEASES
84871  |  AGBL4  |  1.002  |  DISEASES
113146  |  AHNAK2  |  1.172  |  DISEASES
113146  |  AHNAK2  |  1.134  |  DISEASES
84335  |  AKT1S1  |  1.419  |  DISEASES
84335  |  AKT1S1  |  1.381  |  DISEASES
208  |  AKT2  |  1.028  |  DISEASES
223  |  ALDH9A1  |  1.627  |  DISEASES
223  |  ALDH9A1  |  1.589  |  DISEASES
238  |  ALK  |  2.707  |  DISEASES
238  |  ALK  |  2.704  |  DISEASES
23600  |  AMACR  |  5.026  |  DISEASES
23600  |  AMACR  |  5.025  |  DISEASES
154796  |  AMOT  |  1.805  |  DISEASES
154796  |  AMOT  |  1.767  |  DISEASES
283  |  ANG  |  1.03  |  DISEASES
284  |  ANGPT1  |  1.551  |  DISEASES
284  |  ANGPT1  |  1.513  |  DISEASES
26057  |  ANKRD17  |  1.096  |  DISEASES
26057  |  ANKRD17  |  1.058  |  DISEASES
353322  |  ANKRD37  |  1.916  |  DISEASES
353322  |  ANKRD37  |  1.878  |  DISEASES
157567  |  ANKRD46  |  1.056  |  DISEASES
157567  |  ANKRD46  |  1.018  |  DISEASES
302  |  ANXA2  |  2.52  |  DISEASES
302  |  ANXA2  |  2.471  |  DISEASES
307  |  ANXA4  |  1.866  |  DISEASES
307  |  ANXA4  |  1.828  |  DISEASES
317  |  APAF1  |  1.844  |  DISEASES
317  |  APAF1  |  1.74  |  DISEASES
367  |  AR  |  1.956  |  DISEASES
367  |  AR  |  1.918  |  DISEASES
9824  |  ARHGAP11A  |  1.125  |  DISEASES
9824  |  ARHGAP11A  |  1.087  |  DISEASES
8289  |  ARID1A  |  2.409  |  DISEASES
8289  |  ARID1A  |  2.404  |  DISEASES
405  |  ARNT  |  1.597  |  DISEASES
405  |  ARNT  |  1.398  |  DISEASES
9474  |  ATG5  |  1.096  |  DISEASES
9474  |  ATG5  |  1.058  |  DISEASES
533  |  ATP6V0B  |  1.44  |  DISEASES
533  |  ATP6V0B  |  1.403  |  DISEASES
567  |  B2M  |  2.816  |  DISEASES
567  |  B2M  |  2.627  |  DISEASES
2683  |  B4GALT1  |  1.224  |  DISEASES
2683  |  B4GALT1  |  1.186  |  DISEASES
8314  |  BAP1  |  3.965  |  DISEASES
8314  |  BAP1  |  3.927  |  DISEASES
56647  |  BCCIP  |  1.57  |  DISEASES
56647  |  BCCIP  |  1.532  |  DISEASES
10018  |  BCL2L11  |  1.635  |  DISEASES
10018  |  BCL2L11  |  1.301  |  DISEASES
8678  |  BECN1  |  1.334  |  DISEASES
8678  |  BECN1  |  1.296  |  DISEASES
648  |  BMI1  |  1.12  |  DISEASES
648  |  BMI1  |  1.082  |  DISEASES
664  |  BNIP3  |  1.82  |  DISEASES
664  |  BNIP3  |  1.782  |  DISEASES
670  |  BPHL  |  1.315  |  DISEASES
670  |  BPHL  |  1.277  |  DISEASES
100302650  |  BRE-AS1  |  2.199  |  DISEASES
100302650  |  BRE-AS1  |  2.161  |  DISEASES
55845  |  BRK1  |  2.701  |  DISEASES
55845  |  BRK1  |  2.663  |  DISEASES
682  |  BSG  |  2.376  |  DISEASES
682  |  BSG  |  2.253  |  DISEASES
10950  |  BTG3  |  1.021  |  DISEASES
151888  |  BTLA  |  1.094  |  DISEASES
151888  |  BTLA  |  1.056  |  DISEASES
28970  |  C11orf54  |  1.574  |  DISEASES
28970  |  C11orf54  |  1.536  |  DISEASES
201725  |  C4orf46  |  2.282  |  DISEASES
201725  |  C4orf46  |  2.244  |  DISEASES
728  |  C5AR1  |  1.043  |  DISEASES
728  |  C5AR1  |  1.005  |  DISEASES
23632  |  CA14  |  1.035  |  DISEASES
768  |  CA9  |  6.26  |  DISEASES
768  |  CA9  |  6.258  |  DISEASES
27101  |  CACYBP  |  1.126  |  DISEASES
27101  |  CACYBP  |  1.088  |  DISEASES
796  |  CALCA  |  1.623  |  DISEASES
796  |  CALCA  |  1.473  |  DISEASES
800  |  CALD1  |  1.466  |  DISEASES
800  |  CALD1  |  1.428  |  DISEASES
10487  |  CAP1  |  1.018  |  DISEASES
841  |  CASP8  |  2.278  |  DISEASES
841  |  CASP8  |  2.254  |  DISEASES
842  |  CASP9  |  2.279  |  DISEASES
842  |  CASP9  |  2.118  |  DISEASES
857  |  CAV1  |  2.497  |  DISEASES
857  |  CAV1  |  2.459  |  DISEASES
896  |  CCND3  |  1.503  |  DISEASES
896  |  CCND3  |  1.348  |  DISEASES
10693  |  CCT6B  |  1.567  |  DISEASES
10693  |  CCT6B  |  1.529  |  DISEASES
9332  |  CD163  |  1.346  |  DISEASES
9332  |  CD163  |  1.308  |  DISEASES
930  |  CD19  |  1.106  |  DISEASES
930  |  CD19  |  1.069  |  DISEASES
911  |  CD1C  |  1.348  |  DISEASES
911  |  CD1C  |  1.31  |  DISEASES
919  |  CD247  |  1.707  |  DISEASES
919  |  CD247  |  1.669  |  DISEASES
29126  |  CD274  |  4.675  |  DISEASES
29126  |  CD274  |  4.666  |  DISEASES
958  |  CD40  |  1.664  |  DISEASES
958  |  CD40  |  1.626  |  DISEASES
959  |  CD40LG  |  1.184  |  DISEASES
959  |  CD40LG  |  1.078  |  DISEASES
960  |  CD44  |  2.937  |  DISEASES
960  |  CD44  |  2.93  |  DISEASES
965  |  CD58  |  1.222  |  DISEASES
965  |  CD58  |  1.184  |  DISEASES
923  |  CD6  |  3.224  |  DISEASES
923  |  CD6  |  3.204  |  DISEASES
9308  |  CD83  |  2.732  |  DISEASES
9308  |  CD83  |  2.694  |  DISEASES
942  |  CD86  |  2.386  |  DISEASES
942  |  CD86  |  2.378  |  DISEASES
56882  |  CDC42SE1  |  1.337  |  DISEASES
56882  |  CDC42SE1  |  1.299  |  DISEASES
79577  |  CDC73  |  1.509  |  DISEASES
79577  |  CDC73  |  1.471  |  DISEASES
983  |  CDK1  |  1.863  |  DISEASES
983  |  CDK1  |  1.572  |  DISEASES
1029  |  CDKN2A  |  2.813  |  DISEASES
1029  |  CDKN2A  |  2.672  |  DISEASES
1045  |  CDX2  |  1.108  |  DISEASES
5119  |  CHMP1A  |  1.028  |  DISEASES
1366  |  CLDN7  |  2.965  |  DISEASES
1366  |  CLDN7  |  2.927  |  DISEASES
387836  |  CLEC2A  |  1.157  |  DISEASES
387836  |  CLEC2A  |  1.119  |  DISEASES
146223  |  CMTM4  |  1.691  |  DISEASES
146223  |  CMTM4  |  1.653  |  DISEASES
80781  |  COL18A1  |  2.965  |  DISEASES
80781  |  COL18A1  |  2.748  |  DISEASES
84940  |  CORO6  |  1.816  |  DISEASES
84940  |  CORO6  |  1.778  |  DISEASES
1382  |  CRABP2  |  1.369  |  DISEASES
1382  |  CRABP2  |  1.331  |  DISEASES
1385  |  CREB1  |  1.2  |  DISEASES
1385  |  CREB1  |  1.114  |  DISEASES
1435  |  CSF1  |  1.313  |  DISEASES
1435  |  CSF1  |  1.009  |  DISEASES
1485  |  CTAG1B  |  2.011  |  DISEASES
1485  |  CTAG1B  |  1.973  |  DISEASES
1499  |  CTNNB1  |  3.45  |  DISEASES
1499  |  CTNNB1  |  3.356  |  DISEASES
8454  |  CUL1  |  1.81  |  DISEASES
8454  |  CUL1  |  1.772  |  DISEASES
8453  |  CUL2  |  4.113  |  DISEASES
8453  |  CUL2  |  3.863  |  DISEASES
6387  |  CXCL12  |  2.326  |  DISEASES
6387  |  CXCL12  |  2.312  |  DISEASES
9547  |  CXCL14  |  1.783  |  DISEASES
9547  |  CXCL14  |  1.519  |  DISEASES
4283  |  CXCL9  |  2.137  |  DISEASES
4283  |  CXCL9  |  2.099  |  DISEASES
2833  |  CXCR3  |  2.391  |  DISEASES
2833  |  CXCR3  |  2.353  |  DISEASES
7852  |  CXCR4  |  2.783  |  DISEASES
7852  |  CXCR4  |  2.711  |  DISEASES
80319  |  CXXC4  |  1.695  |  DISEASES
80319  |  CXXC4  |  1.657  |  DISEASES
1543  |  CYP1A1  |  1.725  |  DISEASES
1543  |  CYP1A1  |  1.457  |  DISEASES
1565  |  CYP2D6  |  1.044  |  DISEASES
1565  |  CYP2D6  |  1.006  |  DISEASES
1576  |  CYP3A4  |  1.837  |  DISEASES
1576  |  CYP3A4  |  1.788  |  DISEASES
284541  |  CYP4A22  |  1.174  |  DISEASES
284541  |  CYP4A22  |  1.137  |  DISEASES
1612  |  DAPK1  |  1.678  |  DISEASES
1612  |  DAPK1  |  1.641  |  DISEASES
1630  |  DCC  |  1.191  |  DISEASES
1630  |  DCC  |  1.153  |  DISEASES
168400  |  DDX53  |  1.817  |  DISEASES
168400  |  DDX53  |  1.611  |  DISEASES
1676  |  DFFA  |  1.102  |  DISEASES
1676  |  DFFA  |  1.064  |  DISEASES
56616  |  DIABLO  |  1.036  |  DISEASES
23405  |  DICER1  |  1.421  |  DISEASES
23405  |  DICER1  |  1.383  |  DISEASES
7266  |  DNAJC7  |  1.417  |  DISEASES
7266  |  DNAJC7  |  1.379  |  DISEASES
1786  |  DNMT1  |  2.076  |  DISEASES
1786  |  DNMT1  |  1.939  |  DISEASES
1789  |  DNMT3B  |  1.151  |  DISEASES
1791  |  DNTT  |  1.875  |  DISEASES
1791  |  DNTT  |  1.774  |  DISEASES
1803  |  DPP4  |  1.121  |  DISEASES
1803  |  DPP4  |  1.083  |  DISEASES
1869  |  E2F1  |  1.355  |  DISEASES
1869  |  E2F1  |  1.317  |  DISEASES
9166  |  EBAG9  |  1.04  |  DISEASES
9166  |  EBAG9  |  1.002  |  DISEASES
10969  |  EBNA1BP2  |  1.108  |  DISEASES
10969  |  EBNA1BP2  |  1.07  |  DISEASES
1906  |  EDN1  |  1.214  |  DISEASES
1906  |  EDN1  |  1.165  |  DISEASES
54583  |  EGLN1  |  1.821  |  DISEASES
54583  |  EGLN1  |  1.783  |  DISEASES
1977  |  EIF4E  |  1.546  |  DISEASES
1977  |  EIF4E  |  1.508  |  DISEASES
1978  |  EIF4EBP1  |  3.04  |  DISEASES
1978  |  EIF4EBP1  |  3.002  |  DISEASES
1994  |  ELAVL1  |  1.584  |  DISEASES
1994  |  ELAVL1  |  1.561  |  DISEASES
2022  |  ENG  |  2.552  |  DISEASES
2022  |  ENG  |  2.469  |  DISEASES
23136  |  EPB41L3  |  1.157  |  DISEASES
23136  |  EPB41L3  |  1.12  |  DISEASES
1969  |  EPHA2  |  1.841  |  DISEASES
1969  |  EPHA2  |  1.803  |  DISEASES
2047  |  EPHB1  |  1.206  |  DISEASES
2047  |  EPHB1  |  1.168  |  DISEASES
3266  |  ERAS  |  1.744  |  DISEASES
3266  |  ERAS  |  1.653  |  DISEASES
2066  |  ERBB4  |  1.057  |  DISEASES
83715  |  ESPN  |  1.689  |  DISEASES
83715  |  ESPN  |  1.651  |  DISEASES
2130  |  EWSR1  |  1.013  |  DISEASES
7430  |  EZR  |  1.077  |  DISEASES
2173  |  FABP7  |  3.082  |  DISEASES
2173  |  FABP7  |  3.044  |  DISEASES
3992  |  FADS1  |  1.601  |  DISEASES
3992  |  FADS1  |  1.563  |  DISEASES
11170  |  FAM107A  |  2.662  |  DISEASES
11170  |  FAM107A  |  2.624  |  DISEASES
116496  |  FAM129A  |  2.435  |  DISEASES
355  |  FAS  |  2.447  |  DISEASES
355  |  FAS  |  2.247  |  DISEASES
356  |  FASLG  |  2.583  |  DISEASES
356  |  FASLG  |  2.478  |  DISEASES
494188  |  FBXO47  |  1.995  |  DISEASES
494188  |  FBXO47  |  1.958  |  DISEASES
10517  |  FBXW10  |  1.396  |  DISEASES
10517  |  FBXW10  |  1.358  |  DISEASES
2209  |  FCGR1A  |  1.379  |  DISEASES
2209  |  FCGR1A  |  1.236  |  DISEASES
2214  |  FCGR3A  |  3.148  |  DISEASES
2214  |  FCGR3A  |  3.099  |  DISEASES
2246  |  FGF1  |  1.025  |  DISEASES
2258  |  FGF13  |  1.572  |  DISEASES
2258  |  FGF13  |  1.466  |  DISEASES
2260  |  FGFR1  |  2.068  |  DISEASES
2260  |  FGFR1  |  1.86  |  DISEASES
2271  |  FH  |  5.372  |  DISEASES
2271  |  FH  |  5.352  |  DISEASES
2272  |  FHIT  |  3.623  |  DISEASES
2272  |  FHIT  |  3.429  |  DISEASES
2274  |  FHL2  |  1.184  |  DISEASES
2280  |  FKBP1A  |  1.29  |  DISEASES
2335  |  FN1  |  1.084  |  DISEASES
2335  |  FN1  |  1.046  |  DISEASES
96459  |  FNIP1  |  2.694  |  DISEASES
96459  |  FNIP1  |  1.476  |  DISEASES
2300  |  FOXL1  |  1.151  |  DISEASES
2300  |  FOXL1  |  1.113  |  DISEASES
50943  |  FOXP3  |  2.856  |  DISEASES
50943  |  FOXP3  |  2.846  |  DISEASES
143162  |  FRMPD2  |  1.932  |  DISEASES
143162  |  FRMPD2  |  1.894  |  DISEASES
6624  |  FSCN1  |  1.561  |  DISEASES
6624  |  FSCN1  |  1.421  |  DISEASES
170384  |  FUT11  |  1.723  |  DISEASES
170384  |  FUT11  |  1.685  |  DISEASES
2526  |  FUT4  |  2.192  |  DISEASES
2526  |  FUT4  |  2.161  |  DISEASES
53828  |  FXYD4  |  1.893  |  DISEASES
53828  |  FXYD4  |  1.855  |  DISEASES
2534  |  FYN  |  1.046  |  DISEASES
51343  |  FZR1  |  1.395  |  DISEASES
51343  |  FZR1  |  1.357  |  DISEASES
2543  |  GAGE1  |  1.066  |  DISEASES
2543  |  GAGE1  |  1.028  |  DISEASES
2576  |  GAGE4  |  1.061  |  DISEASES
2576  |  GAGE4  |  1.023  |  DISEASES
8693  |  GALNT4  |  1.053  |  DISEASES
8693  |  GALNT4  |  1.015  |  DISEASES
2621  |  GAS6  |  1.331  |  DISEASES
2621  |  GAS6  |  1.293  |  DISEASES
2625  |  GATA3  |  2.21  |  DISEASES
2625  |  GATA3  |  2.177  |  DISEASES
50628  |  GEMIN4  |  1.15  |  DISEASES
50628  |  GEMIN4  |  1.112  |  DISEASES
54438  |  GFOD1  |  2.051  |  DISEASES
54438  |  GFOD1  |  2.013  |  DISEASES
728441  |  GGT2  |  1.632  |  DISEASES
728441  |  GGT2  |  1.262  |  DISEASES
2705  |  GJB1  |  2.634  |  DISEASES
2705  |  GJB1  |  2.596  |  DISEASES
2786  |  GNG4  |  1.398  |  DISEASES
2786  |  GNG4  |  1.36  |  DISEASES
2804  |  GOLGB1  |  1.028  |  DISEASES
10457  |  GPNMB  |  1.308  |  DISEASES
10457  |  GPNMB  |  1.081  |  DISEASES
2882  |  GPX7  |  1.103  |  DISEASES
2882  |  GPX7  |  1.065  |  DISEASES
29841  |  GRHL1  |  1.436  |  DISEASES
29841  |  GRHL1  |  1.398  |  DISEASES
56850  |  GRIPAP1  |  1.37  |  DISEASES
56850  |  GRIPAP1  |  1.332  |  DISEASES
2932  |  GSK3B  |  1.205  |  DISEASES
2932  |  GSK3B  |  1.167  |  DISEASES
2934  |  GSN  |  1.958  |  DISEASES
2934  |  GSN  |  1.875  |  DISEASES
2950  |  GSTP1  |  1.651  |  DISEASES
2950  |  GSTP1  |  1.59  |  DISEASES
3014  |  H2AFX  |  1.066  |  DISEASES
26762  |  HAVCR1  |  2.762  |  DISEASES
26762  |  HAVCR1  |  2.725  |  DISEASES
3039  |  HBA1  |  3.335  |  DISEASES
3039  |  HBA1  |  3.329  |  DISEASES
3055  |  HCK  |  1.746  |  DISEASES
3055  |  HCK  |  1.725  |  DISEASES
23462  |  HEY1  |  1.166  |  DISEASES
23462  |  HEY1  |  1.128  |  DISEASES
3091  |  HIF1A  |  4.693  |  DISEASES
3091  |  HIF1A  |  4.619  |  DISEASES
100750247  |  HIF1A-AS2  |  1.9  |  DISEASES
3105  |  HLA-A  |  1.861  |  DISEASES
3105  |  HLA-A  |  1.823  |  DISEASES
3135  |  HLA-G  |  2.304  |  DISEASES
3135  |  HLA-G  |  2.229  |  DISEASES
79366  |  HMGN5  |  1.478  |  DISEASES
79366  |  HMGN5  |  1.44  |  DISEASES
343069  |  HNRNPCL1  |  1.499  |  DISEASES
343069  |  HNRNPCL1  |  1.462  |  DISEASES
11100  |  HNRNPUL1  |  1.126  |  DISEASES
11100  |  HNRNPUL1  |  1.088  |  DISEASES
100124700  |  HOTAIR  |  1.025  |  DISEASES
3227  |  HOXC11  |  1.542  |  DISEASES
3240  |  HP  |  1.371  |  DISEASES
3240  |  HP  |  1.295  |  DISEASES
3320  |  HSP90AA1  |  1.601  |  DISEASES
3320  |  HSP90AA1  |  1.485  |  DISEASES
3316  |  HSPB2  |  1.536  |  DISEASES
3316  |  HSPB2  |  1.446  |  DISEASES
3384  |  ICAM2  |  1.319  |  DISEASES
3384  |  ICAM2  |  1.281  |  DISEASES
3446  |  IFNA10  |  3.089  |  DISEASES
3446  |  IFNA10  |  3.051  |  DISEASES
3451  |  IFNA17  |  2.871  |  DISEASES
3451  |  IFNA17  |  2.818  |  DISEASES
3440  |  IFNA2  |  4.401  |  DISEASES
3440  |  IFNA2  |  4.339  |  DISEASES
3452  |  IFNA21  |  1.344  |  DISEASES
3452  |  IFNA21  |  1.306  |  DISEASES
3443  |  IFNA6  |  1.033  |  DISEASES
3445  |  IFNA8  |  1.585  |  DISEASES
3456  |  IFNB1  |  2.687  |  DISEASES
3456  |  IFNB1  |  2.567  |  DISEASES
3467  |  IFNW1  |  1.178  |  DISEASES
3467  |  IFNW1  |  1.14  |  DISEASES
3481  |  IGF2  |  1.885  |  DISEASES
3481  |  IGF2  |  1.802  |  DISEASES
3486  |  IGFBP3  |  2.155  |  DISEASES
3486  |  IGFBP3  |  2.117  |  DISEASES
3586  |  IL10  |  2.37  |  DISEASES
3586  |  IL10  |  2.334  |  DISEASES
3559  |  IL2RA  |  1.819  |  DISEASES
3559  |  IL2RA  |  1.781  |  DISEASES
3561  |  IL2RG  |  1.542  |  DISEASES
3561  |  IL2RG  |  1.504  |  DISEASES
54891  |  INO80D  |  1.701  |  DISEASES
54891  |  INO80D  |  1.663  |  DISEASES
26173  |  INTS1  |  1.221  |  DISEASES
26173  |  INTS1  |  1.183  |  DISEASES
3684  |  ITGAM  |  2.019  |  DISEASES
3684  |  ITGAM  |  2.001  |  DISEASES
3709  |  ITPR2  |  2.494  |  DISEASES
3709  |  ITPR2  |  2.456  |  DISEASES
3716  |  JAK1  |  1.515  |  DISEASES
3716  |  JAK1  |  1.457  |  DISEASES
3717  |  JAK2  |  1.29  |  DISEASES
3717  |  JAK2  |  1.207  |  DISEASES
3718  |  JAK3  |  1.501  |  DISEASES
3718  |  JAK3  |  1.422  |  DISEASES
3725  |  JUN  |  2.171  |  DISEASES
3725  |  JUN  |  2.121  |  DISEASES
23189  |  KANK1  |  2.865  |  DISEASES
23189  |  KANK1  |  2.827  |  DISEASES
25959  |  KANK2  |  1.387  |  DISEASES
25959  |  KANK2  |  1.349  |  DISEASES
256949  |  KANK3  |  1.947  |  DISEASES
256949  |  KANK3  |  1.909  |  DISEASES
163782  |  KANK4  |  2.304  |  DISEASES
163782  |  KANK4  |  2.266  |  DISEASES
8242  |  KDM5C  |  3.885  |  DISEASES
8242  |  KDM5C  |  3.87  |  DISEASES
8284  |  KDM5D  |  1.394  |  DISEASES
8284  |  KDM5D  |  1.356  |  DISEASES
7403  |  KDM6A  |  2.693  |  DISEASES
7403  |  KDM6A  |  2.691  |  DISEASES
3814  |  KISS1  |  1.175  |  DISEASES
3814  |  KISS1  |  1.137  |  DISEASES
11279  |  KLF8  |  1.99  |  DISEASES
11279  |  KLF8  |  1.623  |  DISEASES
283212  |  KLHL35  |  1.328  |  DISEASES
283212  |  KLHL35  |  1.29  |  DISEASES
100144748  |  KLLN  |  1.502  |  DISEASES
100144748  |  KLLN  |  1.465  |  DISEASES
3875  |  KRT18  |  2.495  |  DISEASES
3875  |  KRT18  |  2.457  |  DISEASES
3880  |  KRT19  |  2.811  |  DISEASES
3880  |  KRT19  |  2.811  |  DISEASES
3885  |  KRT34  |  1.959  |  DISEASES
3885  |  KRT34  |  1.437  |  DISEASES
3855  |  KRT7  |  5.368  |  DISEASES
3855  |  KRT7  |  5.352  |  DISEASES
3932  |  LCK  |  2.013  |  DISEASES
3932  |  LCK  |  1.932  |  DISEASES
3939  |  LDHA  |  2.017  |  DISEASES
3939  |  LDHA  |  1.936  |  DISEASES
3965  |  LGALS9  |  1.587  |  DISEASES
3965  |  LGALS9  |  1.549  |  DISEASES
401253  |  LINC00336  |  2.199  |  DISEASES
401253  |  LINC00336  |  2.161  |  DISEASES
100302640  |  LINC00882  |  1.802  |  DISEASES
100302640  |  LINC00882  |  1.764  |  DISEASES
100506190  |  LINC00963  |  1.844  |  DISEASES
100506190  |  LINC00963  |  1.806  |  DISEASES
440556  |  LINC00982  |  1.539  |  DISEASES
440556  |  LINC00982  |  1.501  |  DISEASES
4017  |  LOXL2  |  1.85  |  DISEASES
4017  |  LOXL2  |  1.812  |  DISEASES
26020  |  LRP10  |  1.517  |  DISEASES
116135  |  LRRC3B  |  1.728  |  DISEASES
116372  |  LYPD1  |  1.8  |  DISEASES
116372  |  LYPD1  |  1.762  |  DISEASES
4100  |  MAGEA1  |  1.562  |  DISEASES
4100  |  MAGEA1  |  1.524  |  DISEASES
4105  |  MAGEA6  |  2.279  |  DISEASES
4105  |  MAGEA6  |  2.241  |  DISEASES
728239  |  MAGED4  |  1.425  |  DISEASES
728239  |  MAGED4  |  1.387  |  DISEASES
378938  |  MALAT1  |  2.212  |  DISEASES
378938  |  MALAT1  |  2.174  |  DISEASES
440738  |  MAP1LC3C  |  1.386  |  DISEASES
5609  |  MAP2K7  |  2.42  |  DISEASES
5609  |  MAP2K7  |  2.395  |  DISEASES
5599  |  MAPK8  |  1.922  |  DISEASES
5599  |  MAPK8  |  1.903  |  DISEASES
2011  |  MARK2  |  1.222  |  DISEASES
4170  |  MCL1  |  2.505  |  DISEASES
4170  |  MCL1  |  1.565  |  DISEASES
10445  |  MCRS1  |  1.55  |  DISEASES
10445  |  MCRS1  |  1.512  |  DISEASES
4193  |  MDM2  |  2.816  |  DISEASES
4193  |  MDM2  |  2.606  |  DISEASES
100507436  |  MICA  |  1.643  |  DISEASES
100507436  |  MICA  |  1.605  |  DISEASES
2315  |  MLANA  |  3.91  |  DISEASES
2315  |  MLANA  |  3.88  |  DISEASES
4311  |  MME  |  5.218  |  DISEASES
4311  |  MME  |  5.196  |  DISEASES
4312  |  MMP1  |  1.375  |  DISEASES
4312  |  MMP1  |  1.337  |  DISEASES
4318  |  MMP9  |  3.206  |  DISEASES
4318  |  MMP9  |  3.172  |  DISEASES
5891  |  MOK  |  3.111  |  DISEASES
5891  |  MOK  |  3.073  |  DISEASES
10232  |  MSLN  |  2.074  |  DISEASES
10232  |  MSLN  |  1.23  |  DISEASES
4495  |  MT1G  |  2.439  |  DISEASES
4495  |  MT1G  |  2.401  |  DISEASES
4496  |  MT1H  |  1.198  |  DISEASES
4496  |  MT1H  |  1.16  |  DISEASES
2475  |  MTOR  |  6.026  |  DISEASES
2475  |  MTOR  |  5.999  |  DISEASES
4582  |  MUC1  |  2.949  |  DISEASES
4582  |  MUC1  |  2.9  |  DISEASES
4609  |  MYC  |  3.318  |  DISEASES
4609  |  MYC  |  3.279  |  DISEASES
729177  |  NBAT1  |  2.298  |  DISEASES
729177  |  NBAT1  |  2.26  |  DISEASES
9612  |  NCOR2  |  1.582  |  DISEASES
9612  |  NCOR2  |  1.544  |  DISEASES
4696  |  NDUFA3  |  1.463  |  DISEASES
4696  |  NDUFA3  |  1.425  |  DISEASES
4697  |  NDUFA4  |  1.741  |  DISEASES
4697  |  NDUFA4  |  1.703  |  DISEASES
56901  |  NDUFA4L2  |  2.831  |  DISEASES
56901  |  NDUFA4L2  |  2.793  |  DISEASES
4707  |  NDUFB1  |  1.363  |  DISEASES
4707  |  NDUFB1  |  1.325  |  DISEASES
283131  |  NEAT1  |  1.233  |  DISEASES
283131  |  NEAT1  |  1.195  |  DISEASES
4739  |  NEDD9  |  1.29  |  DISEASES
4739  |  NEDD9  |  1.252  |  DISEASES
4753  |  NELL2  |  1.495  |  DISEASES
4753  |  NELL2  |  1.457  |  DISEASES
4771  |  NF2  |  1.761  |  DISEASES
4771  |  NF2  |  1.754  |  DISEASES
10725  |  NFAT5  |  1.559  |  DISEASES
10725  |  NFAT5  |  1.521  |  DISEASES
28512  |  NKIRAS1  |  1.654  |  DISEASES
28512  |  NKIRAS1  |  1.616  |  DISEASES
7080  |  NKX2-1  |  2.86  |  DISEASES
7080  |  NKX2-1  |  2.641  |  DISEASES
654364  |  NME1-NME2  |  1.328  |  DISEASES
654364  |  NME1-NME2  |  1.29  |  DISEASES
4831  |  NME2  |  1.913  |  DISEASES
4831  |  NME2  |  1.815  |  DISEASES
283820  |  NOMO2  |  1.559  |  DISEASES
283820  |  NOMO2  |  1.007  |  DISEASES
408050  |  NOMO3  |  1.561  |  DISEASES
408050  |  NOMO3  |  1.009  |  DISEASES
101241892  |  NPTN-IT1  |  1.009  |  DISEASES
2516  |  NR5A1  |  1.376  |  DISEASES
2516  |  NR5A1  |  1.338  |  DISEASES
8828  |  NRP2  |  1.59  |  DISEASES
8828  |  NRP2  |  1.552  |  DISEASES
318  |  NUDT2  |  1.227  |  DISEASES
4926  |  NUMA1  |  1.776  |  DISEASES
4926  |  NUMA1  |  1.738  |  DISEASES
4988  |  OPRM1  |  1.314  |  DISEASES
4988  |  OPRM1  |  1.276  |  DISEASES
93129  |  ORAI3  |  1.412  |  DISEASES
93129  |  ORAI3  |  1.375  |  DISEASES
126014  |  OSCAR  |  1.716  |  DISEASES
126014  |  OSCAR  |  1.678  |  DISEASES
283208  |  P4HA3  |  1.286  |  DISEASES
283208  |  P4HA3  |  1.248  |  DISEASES
135138  |  PACRG  |  1.063  |  DISEASES
135138  |  PACRG  |  1.025  |  DISEASES
101154753  |  PANDAR  |  1.815  |  DISEASES
101154753  |  PANDAR  |  1.777  |  DISEASES
142  |  PARP1  |  2.275  |  DISEASES
142  |  PARP1  |  2.159  |  DISEASES
64098  |  PARVG  |  1.189  |  DISEASES
64098  |  PARVG  |  1.151  |  DISEASES
5076  |  PAX2  |  4.779  |  DISEASES
5076  |  PAX2  |  4.742  |  DISEASES
7849  |  PAX8  |  4.857  |  DISEASES
7849  |  PAX8  |  4.838  |  DISEASES
55193  |  PBRM1  |  5.368  |  DISEASES
55193  |  PBRM1  |  5.362  |  DISEASES
104472713  |  PCAT29  |  1.177  |  DISEASES
104472713  |  PCAT29  |  1.139  |  DISEASES
5100  |  PCDH8  |  1.735  |  DISEASES
5100  |  PCDH8  |  1.383  |  DISEASES
5133  |  PDCD1  |  3.69  |  DISEASES
5133  |  PDCD1  |  3.652  |  DISEASES
80380  |  PDCD1LG2  |  2.885  |  DISEASES
80380  |  PDCD1LG2  |  2.847  |  DISEASES
5155  |  PDGFB  |  1.758  |  DISEASES
5155  |  PDGFB  |  1.683  |  DISEASES
5228  |  PGF  |  1.416  |  DISEASES
5228  |  PGF  |  1.378  |  DISEASES
5241  |  PGR  |  1.947  |  DISEASES
5241  |  PGR  |  1.809  |  DISEASES
440822  |  PIWIL3  |  1.08  |  DISEASES
440822  |  PIWIL3  |  1.042  |  DISEASES
5325  |  PLAGL1  |  1.039  |  DISEASES
5325  |  PLAGL1  |  1.001  |  DISEASES
5328  |  PLAU  |  1.858  |  DISEASES
5328  |  PLAU  |  1.82  |  DISEASES
5329  |  PLAUR  |  1.017  |  DISEASES
126520  |  PLK5  |  1.245  |  DISEASES
126520  |  PLK5  |  1.207  |  DISEASES
57125  |  PLXDC1  |  1.426  |  DISEASES
57125  |  PLXDC1  |  1.388  |  DISEASES
6490  |  PMEL  |  1.589  |  DISEASES
6490  |  PMEL  |  1.551  |  DISEASES
728378  |  POTEF  |  1.585  |  DISEASES
728378  |  POTEF  |  1.547  |  DISEASES
5454  |  POU3F2  |  1.223  |  DISEASES
5454  |  POU3F2  |  1.185  |  DISEASES
23532  |  PRAME  |  1.972  |  DISEASES
23532  |  PRAME  |  1.934  |  DISEASES
8842  |  PROM1  |  1.913  |  DISEASES
8842  |  PROM1  |  1.803  |  DISEASES
5696  |  PSMB8  |  2.261  |  DISEASES
5696  |  PSMB8  |  2.223  |  DISEASES
5698  |  PSMB9  |  2.23  |  DISEASES
5698  |  PSMB9  |  2.192  |  DISEASES
5725  |  PTBP1  |  1.238  |  DISEASES
58155  |  PTBP2  |  1.38  |  DISEASES
5728  |  PTEN  |  3.7  |  DISEASES
5728  |  PTEN  |  3.655  |  DISEASES
5743  |  PTGS2  |  2.352  |  DISEASES
5743  |  PTGS2  |  2.325  |  DISEASES
5744  |  PTHLH  |  2.83  |  DISEASES
5744  |  PTHLH  |  2.582  |  DISEASES
5747  |  PTK2  |  1.808  |  DISEASES
5747  |  PTK2  |  1.695  |  DISEASES
5788  |  PTPRC  |  1.847  |  DISEASES
5788  |  PTPRC  |  1.846  |  DISEASES
5793  |  PTPRG  |  1.988  |  DISEASES
5793  |  PTPRG  |  1.651  |  DISEASES
9232  |  PTTG1  |  1.052  |  DISEASES
9232  |  PTTG1  |  1.014  |  DISEASES
5820  |  PVT1  |  1.025  |  DISEASES
57111  |  RAB25  |  1.912  |  DISEASES
57111  |  RAB25  |  1.874  |  DISEASES
326624  |  RAB37  |  1.757  |  DISEASES
326624  |  RAB37  |  1.719  |  DISEASES
138046  |  RALYL  |  2.271  |  DISEASES
138046  |  RALYL  |  2.233  |  DISEASES
5915  |  RARB  |  1.424  |  DISEASES
5915  |  RARB  |  1.386  |  DISEASES
11186  |  RASSF1  |  3.014  |  DISEASES
11186  |  RASSF1  |  2.976  |  DISEASES
8241  |  RBM10  |  1.114  |  DISEASES
8241  |  RBM10  |  1.076  |  DISEASES
1104  |  RCC1  |  2.081  |  DISEASES
1104  |  RCC1  |  2.043  |  DISEASES
55920  |  RCC2  |  2.215  |  DISEASES
55920  |  RCC2  |  2.177  |  DISEASES
5970  |  RELA  |  1.698  |  DISEASES
5970  |  RELA  |  1.66  |  DISEASES
5979  |  RET  |  2.484  |  DISEASES
5979  |  RET  |  2.48  |  DISEASES
387  |  RHOA  |  2.355  |  DISEASES
387  |  RHOA  |  2.336  |  DISEASES
253260  |  RICTOR  |  1.573  |  DISEASES
253260  |  RICTOR  |  1.535  |  DISEASES
7732  |  RNF112  |  2.172  |  DISEASES
7732  |  RNF112  |  2.134  |  DISEASES
91445  |  RNF185  |  1.676  |  DISEASES
91445  |  RNF185  |  1.638  |  DISEASES
6093  |  ROCK1  |  1.096  |  DISEASES
6093  |  ROCK1  |  1.058  |  DISEASES
6175  |  RPLP0  |  2.082  |  DISEASES
6175  |  RPLP0  |  2.044  |  DISEASES
6194  |  RPS6  |  1.923  |  DISEASES
6194  |  RPS6  |  1.885  |  DISEASES
58528  |  RRAGD  |  1.215  |  DISEASES
58528  |  RRAGD  |  1.177  |  DISEASES
25950  |  RWDD3  |  1.034  |  DISEASES
6256  |  RXRA  |  1.127  |  DISEASES
6256  |  RXRA  |  1.089  |  DISEASES
6275  |  S100A4  |  1.011  |  DISEASES
6276  |  S100A5  |  1.02  |  DISEASES
6288  |  SAA1  |  1.068  |  DISEASES
6288  |  SAA1  |  1.03  |  DISEASES
6304  |  SATB1  |  1.371  |  DISEASES
6304  |  SATB1  |  1.333  |  DISEASES
60485  |  SAV1  |  1.99  |  DISEASES
60485  |  SAV1  |  1.952  |  DISEASES
6319  |  SCD  |  1.173  |  DISEASES
6319  |  SCD  |  1.135  |  DISEASES
10590  |  SCGN  |  1.163  |  DISEASES
10590  |  SCGN  |  1.125  |  DISEASES
29970  |  SCHIP1  |  1.835  |  DISEASES
29970  |  SCHIP1  |  1.797  |  DISEASES
6390  |  SDHB  |  3.669  |  DISEASES
6390  |  SDHB  |  3.507  |  DISEASES
6391  |  SDHC  |  2.863  |  DISEASES
6391  |  SDHC  |  2.584  |  DISEASES
6392  |  SDHD  |  2.938  |  DISEASES
6392  |  SDHD  |  2.777  |  DISEASES
6401  |  SELE  |  1.519  |  DISEASES
6401  |  SELE  |  1.38  |  DISEASES
54437  |  SEMA5B  |  1.419  |  DISEASES
54437  |  SEMA5B  |  1.381  |  DISEASES
5265  |  SERPINA1  |  1.036  |  DISEASES
29072  |  SETD2  |  4.613  |  DISEASES
29072  |  SETD2  |  4.583  |  DISEASES
84193  |  SETD3  |  2.256  |  DISEASES
84193  |  SETD3  |  2.218  |  DISEASES
2810  |  SFN  |  1.111  |  DISEASES
6421  |  SFPQ  |  2.664  |  DISEASES
6421  |  SFPQ  |  2.626  |  DISEASES
27036  |  SIGLEC7  |  2.483  |  DISEASES
27036  |  SIGLEC7  |  2.445  |  DISEASES
9123  |  SLC16A3  |  2.427  |  DISEASES
9123  |  SLC16A3  |  2.411  |  DISEASES
26503  |  SLC17A5  |  2.507  |  DISEASES
26503  |  SLC17A5  |  2.469  |  DISEASES
6513  |  SLC2A1  |  3.106  |  DISEASES
6513  |  SLC2A1  |  3.098  |  DISEASES
6518  |  SLC2A5  |  1.058  |  DISEASES
6518  |  SLC2A5  |  1.02  |  DISEASES
80723  |  SLC35G2  |  2.488  |  DISEASES
80723  |  SLC35G2  |  2.45  |  DISEASES
201266  |  SLC39A11  |  1.576  |  DISEASES
201266  |  SLC39A11  |  1.538  |  DISEASES
204962  |  SLC44A5  |  2.814  |  DISEASES
204962  |  SLC44A5  |  2.776  |  DISEASES
9353  |  SLIT2  |  1.351  |  DISEASES
9353  |  SLIT2  |  1.313  |  DISEASES
6586  |  SLIT3  |  1.218  |  DISEASES
6586  |  SLIT3  |  1.18  |  DISEASES
4089  |  SMAD4  |  1.213  |  DISEASES
4089  |  SMAD4  |  1.175  |  DISEASES
6597  |  SMARCA4  |  1.278  |  DISEASES
6597  |  SMARCA4  |  1.011  |  DISEASES
643008  |  SMIM5  |  2.229  |  DISEASES
643008  |  SMIM5  |  2.191  |  DISEASES
55627  |  SMPD4  |  1.489  |  DISEASES
55627  |  SMPD4  |  1.451  |  DISEASES
23583  |  SMUG1  |  3.801  |  DISEASES
23583  |  SMUG1  |  3.794  |  DISEASES
84973  |  SNHG7  |  1.896  |  DISEASES
84973  |  SNHG7  |  1.858  |  DISEASES
26821  |  SNORA74A  |  1.748  |  DISEASES
26821  |  SNORA74A  |  1.71  |  DISEASES
727676  |  SNORD118  |  1.891  |  DISEASES
677848  |  SNORD1A  |  1.653  |  DISEASES
677848  |  SNORD1A  |  1.616  |  DISEASES
26806  |  SNORD44  |  1.946  |  DISEASES
26806  |  SNORD44  |  1.908  |  DISEASES
26801  |  SNORD48  |  1.225  |  DISEASES
26801  |  SNORD48  |  1.187  |  DISEASES
619498  |  SNORD74  |  1.374  |  DISEASES
619498  |  SNORD74  |  1.336  |  DISEASES
64089  |  SNX16  |  1.12  |  DISEASES
64089  |  SNX16  |  1.082  |  DISEASES
6676  |  SPAG4  |  2.342  |  DISEASES
6676  |  SPAG4  |  2.304  |  DISEASES
153218  |  SPINK13  |  1.305  |  DISEASES
153218  |  SPINK13  |  1.267  |  DISEASES
6696  |  SPP1  |  2.025  |  DISEASES
6696  |  SPP1  |  2  |  DISEASES
6714  |  SRC  |  2.862  |  DISEASES
6714  |  SRC  |  2.615  |  DISEASES
727837  |  SSX2B  |  1.859  |  DISEASES
727837  |  SSX2B  |  1.821  |  DISEASES
6772  |  STAT1  |  1.661  |  DISEASES
6772  |  STAT1  |  1.574  |  DISEASES
6776  |  STAT5A  |  1.226  |  DISEASES
6776  |  STAT5A  |  1.188  |  DISEASES
55959  |  SULF2  |  1.28  |  DISEASES
140732  |  SUN5  |  1.667  |  DISEASES
140732  |  SUN5  |  1.629  |  DISEASES
85360  |  SYDE1  |  1.093  |  DISEASES
85360  |  SYDE1  |  1.055  |  DISEASES
148281  |  SYT6  |  1.319  |  DISEASES
148281  |  SYT6  |  1.281  |  DISEASES
4943  |  TBC1D25  |  1.516  |  DISEASES
4943  |  TBC1D25  |  1.478  |  DISEASES
11138  |  TBC1D8  |  1.472  |  DISEASES
11138  |  TBC1D8  |  1.434  |  DISEASES
27004  |  TCL6  |  1.138  |  DISEASES
27004  |  TCL6  |  1.1  |  DISEASES
7005  |  TEAD3  |  1.135  |  DISEASES
7005  |  TEAD3  |  1.097  |  DISEASES
7010  |  TEK  |  2.477  |  DISEASES
7010  |  TEK  |  2.369  |  DISEASES
7045  |  TGFBI  |  1.786  |  DISEASES
7045  |  TGFBI  |  1.748  |  DISEASES
7046  |  TGFBR1  |  1.054  |  DISEASES
7052  |  TGM2  |  1.574  |  DISEASES
7052  |  TGM2  |  1.536  |  DISEASES
7068  |  THRB  |  1.796  |  DISEASES
7068  |  THRB  |  1.758  |  DISEASES
54106  |  TLR9  |  1.407  |  DISEASES
54106  |  TLR9  |  1.012  |  DISEASES
79838  |  TMC5  |  1.413  |  DISEASES
79838  |  TMC5  |  1.375  |  DISEASES
89894  |  TMEM116  |  2.229  |  DISEASES
89894  |  TMEM116  |  2.191  |  DISEASES
131920  |  TMEM207  |  1.212  |  DISEASES
131920  |  TMEM207  |  1.174  |  DISEASES
155006  |  TMEM213  |  2.803  |  DISEASES
155006  |  TMEM213  |  2.765  |  DISEASES
161291  |  TMEM30B  |  1.162  |  DISEASES
161291  |  TMEM30B  |  1.125  |  DISEASES
200197  |  TMEM51-AS1  |  2.199  |  DISEASES
200197  |  TMEM51-AS1  |  2.161  |  DISEASES
199964  |  TMEM61  |  1.831  |  DISEASES
199964  |  TMEM61  |  1.793  |  DISEASES
643236  |  TMEM72  |  1.861  |  DISEASES
643236  |  TMEM72  |  1.823  |  DISEASES
7114  |  TMSB4X  |  1.189  |  DISEASES
7114  |  TMSB4X  |  1.151  |  DISEASES
7124  |  TNF  |  3.331  |  DISEASES
7124  |  TNF  |  3.224  |  DISEASES
3604  |  TNFRSF9  |  1.337  |  DISEASES
7150  |  TOP1  |  1.27  |  DISEASES
7150  |  TOP1  |  1.058  |  DISEASES
7162  |  TPBG  |  3.462  |  DISEASES
7162  |  TPBG  |  3.424  |  DISEASES
7170  |  TPM3  |  1.372  |  DISEASES
7170  |  TPM3  |  1.334  |  DISEASES
7171  |  TPM4  |  1.045  |  DISEASES
7171  |  TPM4  |  1.007  |  DISEASES
388630  |  TRABD2B  |  1.516  |  DISEASES
388630  |  TRABD2B  |  1.478  |  DISEASES
7185  |  TRAF1  |  1.171  |  DISEASES
7185  |  TRAF1  |  1.133  |  DISEASES
7187  |  TRAF3  |  1.816  |  DISEASES
7187  |  TRAF3  |  1.645  |  DISEASES
100507602  |  TRIM52-AS1  |  2.282  |  DISEASES
100507602  |  TRIM52-AS1  |  2.244  |  DISEASES
80036  |  TRPM3  |  1.403  |  DISEASES
80036  |  TRPM3  |  1.365  |  DISEASES
7102  |  TSPAN7  |  1.037  |  DISEASES
100287898  |  TTC34  |  1.552  |  DISEASES
100287898  |  TTC34  |  1.514  |  DISEASES
55000  |  TUG1  |  1.095  |  DISEASES
55000  |  TUG1  |  1.057  |  DISEASES
286319  |  TUSC1  |  1.165  |  DISEASES
286319  |  TUSC1  |  1.127  |  DISEASES
7295  |  TXN  |  1.105  |  DISEASES
7295  |  TXN  |  1.067  |  DISEASES
81567  |  TXNDC5  |  1.665  |  DISEASES
81567  |  TXNDC5  |  1.627  |  DISEASES
134111  |  UBE2QL1  |  1.546  |  DISEASES
134111  |  UBE2QL1  |  1.508  |  DISEASES
127933  |  UHMK1  |  1.03  |  DISEASES
8408  |  ULK1  |  1.1  |  DISEASES
8408  |  ULK1  |  1.062  |  DISEASES
10975  |  UQCR11  |  1.426  |  DISEASES
10975  |  UQCR11  |  1.388  |  DISEASES
7421  |  VDR  |  1.669  |  DISEASES
7421  |  VDR  |  1.631  |  DISEASES
7422  |  VEGFA  |  5.797  |  DISEASES
7422  |  VEGFA  |  5.779  |  DISEASES
391104  |  VHLL  |  1.578  |  DISEASES
391104  |  VHLL  |  1.54  |  DISEASES
7432  |  VIP  |  1.057  |  DISEASES
7432  |  VIP  |  1.02  |  DISEASES
79679  |  VTCN1  |  3.068  |  DISEASES
79679  |  VTCN1  |  3.03  |  DISEASES
91833  |  WDR20  |  1.296  |  DISEASES
91833  |  WDR20  |  1.258  |  DISEASES
89891  |  WDR34  |  1.138  |  DISEASES
89891  |  WDR34  |  1.1  |  DISEASES
7490  |  WT1  |  3.253  |  DISEASES
7490  |  WT1  |  3.154  |  DISEASES
51741  |  WWOX  |  1.315  |  DISEASES
51741  |  WWOX  |  1.277  |  DISEASES
331  |  XIAP  |  1.539  |  DISEASES
331  |  XIAP  |  1.35  |  DISEASES
2547  |  XRCC6  |  1.265  |  DISEASES
2547  |  XRCC6  |  1.066  |  DISEASES
4904  |  YBX1  |  1.157  |  DISEASES
4904  |  YBX1  |  1.119  |  DISEASES
6935  |  ZEB1  |  1.832  |  DISEASES
6935  |  ZEB1  |  1.794  |  DISEASES
124961  |  ZFP3  |  1.687  |  DISEASES
124961  |  ZFP3  |  1.649  |  DISEASES
23051  |  ZHX3  |  1.393  |  DISEASES
23051  |  ZHX3  |  1.355  |  DISEASES
7694  |  ZNF135  |  2.528  |  DISEASES
7694  |  ZNF135  |  2.43  |  DISEASES
10168  |  ZNF197  |  1.808  |  DISEASES
23567  |  ZNF346  |  1.119  |  DISEASES
23567  |  ZNF346  |  1.081  |  DISEASES
7584  |  ZNF35  |  2.374  |  DISEASES
7584  |  ZNF35  |  1.409  |  DISEASES
57862  |  ZNF410  |  1.511  |  DISEASES
57862  |  ZNF410  |  1.473  |  DISEASES
79744  |  ZNF419  |  1.837  |  DISEASES
79744  |  ZNF419  |  1.799  |  DISEASES
162966  |  ZNF600  |  1.537  |  DISEASES
162966  |  ZNF600  |  1.499  |  DISEASES
30834  |  ZNRD1  |  1.366  |  DISEASES
30834  |  ZNRD1  |  1.328  |  DISEASES
65982  |  ZSCAN18  |  1.085  |  DISEASES
65982  |  ZSCAN18  |  1.047  |  DISEASES
Locus(Waiting for update.)
Disease ID 98
Disease renal cell carcinoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:115)
HP:0002664  |  Neoplasia  |  158
HP:0030731  |  Carcinoma  |  14
HP:0003774  |  End-stage renal failure  |  12
HP:0001513  |  Obesity  |  11
HP:0000822  |  Hypertension  |  11
HP:0012622  |  Chronic kidney disease  |  7
HP:0001907  |  Thromboembolic disease  |  7
HP:0005584  |  Renal cell carcinoma  |  5
HP:0002835  |  Aspiration  |  5
HP:0009726  |  Renal neoplasm  |  4
HP:0001082  |  Cholecystitis  |  4
HP:0012126  |  Gastric cancer  |  4
HP:0002861  |  Melanoma  |  4
HP:0001635  |  Congestive heart failure  |  4
HP:0012531  |  Pain  |  3
HP:0001903  |  Anemia  |  3
HP:0002669  |  Osteosarcoma  |  3
HP:0006766  |  Papillary renal cell carcinoma  |  3
HP:0006772  |  Angiomyolipoma  |  3
HP:0002665  |  Lymphoma  |  3
HP:0000821  |  Underactive thyroid  |  3
HP:0001541  |  Ascites  |  3
HP:0000819  |  Diabetes mellitus  |  3
HP:0012034  |  Liposarcoma  |  3
HP:0001894  |  Thrombocytosis  |  3
HP:0002584  |  Intestinal hemorrhage  |  2
HP:0001945  |  Fever  |  2
HP:0012378  |  Fatigue  |  2
HP:0001217  |  Digital clubbing  |  2
HP:0000979  |  Purpura  |  2
HP:0000718  |  Aggressive behaviour  |  2
HP:0000085  |  Horseshoe kidney  |  2
HP:0002633  |  Vasculitis  |  2
HP:0002176  |  Spinal cord compression  |  2
HP:0001919  |  Acute renal failure  |  2
HP:0011798  |  Renal oncocytoma  |  2
HP:0002667  |  Wilms tumor  |  2
HP:0010797  |  Hemangioblastoma  |  2
HP:0003072  |  Hypercalcemia  |  2
HP:0000086  |  Ectopic kidney  |  2
HP:0002027  |  Abdominal pain  |  2
HP:0000113  |  Polycystic kidney dysplasia  |  2
HP:0000083  |  Renal insufficiency  |  2
HP:0000107  |  Renal cyst  |  2
HP:0006770  |  Nonpapillary renal cell carcinoma  |  2
HP:0100759  |  Finger clubbing  |  1
HP:0009725  |  Bladder neoplasm  |  1
HP:0005200  |  Retroperitoneal fibrosis  |  1
HP:0000999  |  Pyoderma  |  1
HP:0003473  |  Fatigable weakness  |  1
HP:0002105  |  Hemoptysis  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0001396  |  Cholestasis  |  1
HP:0003073  |  Hypoalbuminaemia  |  1
HP:0005306  |  Capillary hemangioma  |  1
HP:0001901  |  Abnormally shaped erythrocytes  |  1
HP:0008221  |  Enlarged adrenal glands  |  1
HP:0008200  |  Primary hyperparathyroidism  |  1
HP:0012156  |  Hemophagocytosis  |  1
HP:0002893  |  Pituitary adenoma  |  1
HP:0012636  |  Retinal vein occlusion  |  1
HP:0011974  |  Myelofibrosis  |  1
HP:0000093  |  Proteinuria  |  1
HP:0002902  |  Hyponatremia  |  1
HP:0000738  |  Sensory hallucination  |  1
HP:0000787  |  Renal calculi  |  1
HP:0009733  |  Glioma  |  1
HP:0002647  |  Aortic dissection  |  1
HP:0001289  |  Confusion  |  1
HP:0005145  |  Narrowing of coronary artery  |  1
HP:0003765  |  Psoriasis  |  1
HP:0100697  |  Neurofibrosarcoma  |  1
HP:0002896  |  Liver cancer  |  1
HP:0100727  |  Histiocytosis  |  1
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0100633  |  Inflammation of the esophagus  |  1
HP:0000421  |  Bloody nose  |  1
HP:0002204  |  Pulmonary embolism  |  1
HP:0002890  |  Thyroid carcinoma  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0001297  |  Cerebral vascular events  |  1
HP:0011349  |  Sixth nerve palsy  |  1
HP:0000843  |  Hyperparathyroidism  |  1
HP:0000100  |  Nephrosis  |  1
HP:0100665  |  Angiooedema  |  1
HP:0008258  |  Congenital adrenal hyperplasia  |  1
HP:0001004  |  Lymphatic obstruction  |  1
HP:0001978  |  Extramedullary hematopoiesis  |  1
HP:0002239  |  Gastrointestinal hemorrhage  |  1
HP:0010566  |  Hamartoma  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0001402  |  Hepatocellular carcinoma  |  1
HP:0002249  |  Melena  |  1
HP:0002894  |  Neoplasia of the pancreas  |  1
HP:0002015  |  Swallowing difficulty  |  1
HP:0100658  |  Bacterial infection of skin  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0002668  |  Paragangliomas  |  1
HP:0001369  |  Arthritis  |  1
HP:0000952  |  Yellow skin  |  1
HP:0200023  |  Priapism  |  1
HP:0000131  |  Uterine leiomyoma  |  1
HP:0002090  |  Pneumonia  |  1
HP:0002901  |  Hypocalcemia  |  1
HP:0001882  |  Decreased blood leukocyte number  |  1
HP:0030839  |  Knee pain  |  1
HP:0003201  |  Rhabdomyolysis  |  1
HP:0001028  |  Strawberry mark  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0002576  |  Intussusception  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0030242  |  Blood clot in portal vein  |  1
HP:0001138  |  Damaged optic nerve  |  1
Disease ID 98
Disease renal cell carcinoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:145)
C2697391  |  rheumatoid arthritis
C2613439  |  extramedullary hematopoiesis
C2598155  |  pain
C2248595  |  dedifferentiation
C2173677  |  renal cyst
C2119038  |  pleural metastasis
C2073625  |  pleural effusion
C2039684  |  systemic symptoms
C1963185  |  obesity
C1962972  |  proteinuria
C1840264  |  immune suppression
C1839611  |  n syndrome
C1691228  |  cystic disease of kidney
C1609519  |  adrenal myelolipoma
C1608408  |  malignant transformation
C1550639  |  fistula
C1516669  |  clonal evolution
C1510885  |  angiogenic switch
C1415107  |  stiff person syndrome
C1335751  |  inverted papilloma of the renal pelvis
C1335745  |  renal liposarcoma
C1332900  |  cerebellar hemangioblastoma
C1332335  |  arterial embolization
C1321756  |  achalasia
C1306459  |  primary malignant neoplasm
C1142517  |  lupus anticoagulant
C1135207  |  ataxia
C1000587  |  pemphigus
C1000483  |  anemia
C0878650  |  stauffer's syndrome
C0878544  |  cardiomyopathy
C0854178  |  adrenal metastases
C0836924  |  thrombocytosis
C0741299  |  atrial thrombus
C0686619  |  lymph node metastases
C0684817  |  neck metastasis
C0684550  |  spinal metastases
C0555278  |  cerebral metastases
C0521607  |  peritoneal fibrosis
C0497156  |  lymphadenopathy
C0494165  |  metastasis to liver
C0494165  |  liver metastasis
C0494165  |  liver metastases
C0494165  |  hepatic metastasis
C0424755  |  fever
C0406650  |  linear iga bullous dermatosis
C0403416  |  crescentic glomerulonephritis
C0401040  |  retroperitoneal fat necrosis
C0398359  |  trousseau's syndrome
C0347005  |  scrotal metastasis
C0346993  |  breast metastasis
C0346993  |  breast metastases
C0346976  |  pancreatic metastasis
C0346255  |  renal oncocytoma
C0334121  |  inflammatory myofibroblastic tumor
C0333516  |  tumor necrosis
C0302148  |  thrombus
C0271901  |  microcytic hypochromic anemia
C0270612  |  leukoencephalopathy
C0268799  |  acquired renal cystic disease
C0268381  |  primary amyloidosis
C0268381  |  al amyloidosis
C0267373  |  intestinal bleeding
C0265050  |  vena cava thrombosis
C0240225  |  hepatic mass
C0238457  |  renal vein thrombosis
C0235782  |  carcinoma of the gallbladder
C0221002  |  primary hyperparathyroidism
C0220650  |  brain metastasis
C0220650  |  brain metastases
C0206667  |  adrenocortical adenoma
C0206667  |  adrenal adenoma
C0206635  |  myelolipoma
C0206633  |  angiomyolipomas
C0206180  |  anaplastic large cell lymphoma
C0155675  |  pulmonary arteriovenous fistula
C0153690  |  osseous metastasis
C0153690  |  bony metastasis
C0153690  |  bone metastasis
C0153690  |  bone metastases
C0153687  |  skin metastasis
C0153687  |  skin metastases
C0153687  |  cutaneous metastasis
C0153685  |  renal metastasis
C0153676  |  pulmonary metastasis
C0153676  |  pulmonary metastases
C0153676  |  lung metastasis
C0153676  |  lung metastases
C0152244  |  aneurysmal bone cyst
C0152002  |  renal vasculitis
C0151650  |  renal fibrosis
C0087086  |  thrombi
C0085652  |  pyoderma gangrenosum
C0085642  |  livedo reticularis
C0043092  |  wegener's granulomatosis
C0037933  |  spine disease
C0037928  |  myelopathy
C0037284  |  skin lesions
C0036527  |  ovarian metastasis
C0034902  |  pure red cell aplasia
C0034188  |  xanthogranulomatous pyelonephritis
C0034065  |  pulmonary embolism
C0031511  |  adrenal pheochromocytoma
C0030472  |  paraneoplastic syndromes
C0030472  |  paraneoplastic syndrome
C0029896  |  ent disease
C0027149  |  myxoma
C0027123  |  myospherulosis
C0027066  |  myoclonus
C0025470  |  mesenteric lipodystrophy
C0024232  |  lymphatic metastases
C0023903  |  liver tumor
C0023895  |  liver disorder
C0022681  |  medullary sponge kidney
C0022679  |  cystic kidneys
C0022665  |  renal tumors
C0022660  |  acute renal failure
C0022658  |  nephropathy
C0022079  |  iris tumor
C0021308  |  infarction
C0021053  |  immune dysfunction
C0020615  |  hypoglycemia
C0020546  |  hypertensive crisis
C0020456  |  hyperglycemia
C0020437  |  hypercalcemia
C0020437  |  hypercalcaemia
C0019562  |  von hippel-lindau disease
C0019562  |  von hippel lindau disease
C0019080  |  hemorrhage
C0018801  |  heart failure
C0017665  |  membranous nephropathy
C0017665  |  membranous glomerulonephritis
C0017661  |  iga nephropathy
C0017661  |  iga glomerulonephritis
C0014743  |  erythema nodosum
C0014130  |  endocrinopathy
C0013930  |  tumor embolism
C0013292  |  duodenal obstruction
C0009062  |  clostridial infection
C0008497  |  choriocarcinoma
C0007758  |  cerebellar ataxia
C0007138  |  transitional cell carcinoma
C0006625  |  cachexia
C0002736  |  amyotrophic lateral sclerosis
C0002726  |  amyloidosis
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:54)
C0040053  |  thrombus  |  49
C0153690  |  bone metastasis  |  13
C0028754  |  obesity  |  10
C0019562  |  von hippel-lindau disease  |  7
C0153690  |  bone metastases  |  7
C0220650  |  brain metastases  |  6
C0153676  |  lung metastases  |  6
C0002793  |  dedifferentiation  |  6
C0220650  |  brain metastasis  |  5
C0153676  |  pulmonary metastasis  |  5
C0153676  |  lung metastasis  |  5
C1332335  |  arterial embolization  |  4
C0153676  |  pulmonary metastases  |  4
C0022665  |  renal tumors  |  3
C0153687  |  cutaneous metastasis  |  3
C0019562  |  von hippel lindau disease  |  3
C0836924  |  thrombocytosis  |  3
C0153685  |  renal metastasis  |  3
C0018801  |  heart failure  |  3
C0155776  |  renal vein thrombosis  |  2
C0686619  |  lymph node metastases  |  2
C0030193  |  pain  |  2
C0494165  |  liver metastases  |  2
C0020437  |  hypercalcemia  |  2
C0030472  |  paraneoplastic syndrome  |  2
C1335745  |  renal liposarcoma  |  1
C0016169  |  fistula  |  1
C0494165  |  liver metastasis  |  1
C0268799  |  acquired renal cystic disease  |  1
C2119038  |  pleural metastasis  |  1
C0034065  |  pulmonary embolism  |  1
C0027149  |  myxoma  |  1
C0018952  |  extramedullary hematopoiesis  |  1
C0346976  |  pancreatic metastasis  |  1
C0206635  |  myelolipoma  |  1
C0333516  |  tumor necrosis  |  1
C0002871  |  anemia  |  1
C0153687  |  skin metastasis  |  1
C0340539  |  pulmonary tumor embolism  |  1
C0032227  |  pleural effusion  |  1
C0741299  |  atrial thrombus  |  1
C0521607  |  peritoneal fibrosis  |  1
C0023903  |  liver tumor  |  1
C0003873  |  rheumatoid arthritis  |  1
C0346255  |  renal oncocytoma  |  1
C0022679  |  renal cyst  |  1
C0019080  |  hemorrhage  |  1
C0854178  |  adrenal metastases  |  1
C0241961  |  renal angiomyolipoma  |  1
C0020538  |  hypertension  |  1
C0267373  |  intestinal bleeding  |  1
C0085652  |  pyoderma gangrenosum  |  1
C1609519  |  adrenal myelolipoma  |  1
C0015967  |  fever  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:90)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs100545042318415023037PDZD2umls:C0007134GWASCATCommon variation at 2q22.3 (ZEB2) influences the risk of renal cancer.0.1202714422013PDZD2532000377TC
rs1042522176345397157TP53umls:C0007134BeFreePolymorphisms of p53 Arg(72)Pro and p21 Ser(31)Arg did not show significant association with RCC.0.1503553392007TP53177676154GT,C
rs1045642223583025243ABCB1umls:C1378703BeFreeIn summary, this meta-analysis suggests that the MDR1 C3435T polymorphism is associated with cancer susceptibility, increasing the risk of breast and renal cancer.0.0019000932012ABCB1787509329AT,G
rs1049380239116363709ITPR2umls:C0007134BeFreeAfter adjusting for patient age, gender, smoking status and body mass index the AG + AA genotypes from rs7105934 (11q13) were associated with a decreased risk of renal cell carcinoma (OR 0.50, 95% CI 0.33-0.75, p = 0.001) and the AC + CC genotypes from rs1049380 (ITPR2) were associated with an increased risk (OR 1.66, 95% CI 1.28-2.16, p <0.001).0.0008143262013ITPR21226336611GT
rs1049380220100483709ITPR2umls:C0007134BeFreeWe identified two common variants in linkage disequilibrium, rs718314 and rs1049380 (r(2) = 0.64, D ' = 0.84), in the inositol 1,4,5-triphosphate receptor, type 2 (ITPR2) gene on 12p11.23 as novel susceptibility loci for RCC (P = 8.89 × 10(-10) and P = 6.07 × 10(-9), respectively, in meta-analysis) with an allelic odds ratio of 1.19 [95% confidence interval (CI): 1.13-1.26] for rs718314 and 1.18 (95% CI: 1.12-1.25) for rs1049380.0.0008143262012ITPR21226336611GT
rs1052133211664934968OGG1umls:C0007134BeFreehOGG1 Ser326Cys polymorphism and renal cell carcinoma risk in a Chinese population.0.2029957922011OGG1;CAMK139757089CG
rs10771279242209107515XRCC1umls:C0007134BeFreeThe 12p11.23 variant rs10771279, located 77 kb from the European-ancestry RCC marker rs718314, was associated with RCC risk in the GWAS (P = 1.2 × 10(-7)) but did not replicate (P = 0.99).0.0159391262014ITPR21226377610TA,C
rs11022095195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK31111965380AG
rs110220951956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK31111965380AG
rs11348802226014474673BRAFumls:C0007134BeFreeThus, BRAF V600E immunostaining is a helpful marker for pediatric metanephric adenoma, and additional research is required on the possible role of this mutation in the development of renal carcinoma.0.0005428842015BRAF7140753336AT,G,C
rs11348802226014474673BRAFumls:C1378703BeFreeThus, BRAF V600E immunostaining is a helpful marker for pediatric metanephric adenoma, and additional research is required on the possible role of this mutation in the development of renal carcinoma.0.0002714422015BRAF7140753336AT,G,C
rs11540654176345397157TP53umls:C0007134BeFreePolymorphisms of p53 Arg(72)Pro and p21 Ser(31)Arg did not show significant association with RCC.0.1503553392007TP53177676040CT,G,A
rs11549465189494193091HIF1Aumls:C0007134BeFreeIn previous studies, the C1772T (P582S) or the G1790A (A588T) polymorphisms of the HIF-1alpha gene have been identified in renal cell carcinoma, head and neck and esophageal squamous cell carcinomas as well as colorectal and prostate cancers.0.036909672008HIF1A;LOC1053705261461740839CT
rs11549467189494193091HIF1Aumls:C0007134BeFreeIn previous studies, the C1772T (P582S) or the G1790A (A588T) polymorphisms of the HIF-1alpha gene have been identified in renal cell carcinoma, head and neck and esophageal squamous cell carcinomas as well as colorectal and prostate cancers.0.036909672008HIF1A;LOC1053705261461740857GA
rs1161491324681820406938MIR146Aumls:C0007134BeFreemiR-146a rs2910164, miR-149 rs2292832, miR-196a2 rs11614913 and miR-499 rs3746444) to assess their associations with RCC risk in a two-stage case-control study (355 cases and 362 controls in discovery set, meanwhile 647 cases and 660 controls in validation set), as well as RCC survival in 311 patients.0.0026384742014MIR196A21253991815CT
rs11894252211319752034EPAS1umls:C0007134BeFreeTwo correlated variants (r² = 0.99 in controls), rs11894252 (P = 1.8 × 10⁻⁸) and rs7579899 (P = 2.3 × 10⁻⁹), map to EPAS1 on 2p21, which encodes hypoxia-inducible-factor-2 alpha, a transcription factor previously implicated in RCC.0.3327016862011EPAS1;LOC105374583246306237TC
rs12105918231841509839ZEB2umls:C0007134GWASCATOur findings suggest that genetic variation in ZEB2 influences the risk of RCC.0.1213572092013ZEB2;LOC105373659;LOC1053736602144450626TC
rs121913243NA4233METumls:C0007134CLINVARNA0.253320515NAMET7116777410AC,G
rs121913246NA4233METumls:C0007134CLINVARNA0.253320515NAMET7116783360AG
rs121913668NA4233METumls:C0007134CLINVARNA0.253320515NAMET7116778827TC
rs121913669NA4233METumls:C0007134CLINVARNA0.253320515NAMET7116782027GA,T
rs121913670NA4233METumls:C0007134CLINVARNA0.253320515NAMET7116783329GA
rs121913671NA4233METumls:C0007134CLINVARNA0.253320515NAMET7116783353GA
rs121913673NA4233METumls:C0007134CLINVARNA0.253320515NAMET7116782048CG
rs129537171956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009SMAD71848927559CT
rs12953717195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009SMAD71848927559CT
rs132770255696442547XRCC6umls:C0007134BeFreeSensitivity analyses were also performed.The rs2267437 polymorphism was associated with a significant increase in risks of overall cancers, breast cancer, renal cell carcinoma and hepatocellular carcinoma, and it could increase the cancer risk in Asian population; the rs5751129 polymorphism could increase the cancer risk in overall cancers; the rs132770 polymorphism was associated with the increased renal cell carcinoma risk; furthermore, the rs132793 polymorphism could decrease breast cancer risk and increase risks in other cancers.Overall, the results provided evidences that the single nucleotide polymorphisms in XRCC6 promoter region might play different roles in various cancers, indicating different cancers have different tumorigenesis mechanisms.0.0010857672015XRCC6;DESI12241621260AG
rs132793255696442547XRCC6umls:C0007134BeFreeSensitivity analyses were also performed.The rs2267437 polymorphism was associated with a significant increase in risks of overall cancers, breast cancer, renal cell carcinoma and hepatocellular carcinoma, and it could increase the cancer risk in Asian population; the rs5751129 polymorphism could increase the cancer risk in overall cancers; the rs132770 polymorphism was associated with the increased renal cell carcinoma risk; furthermore, the rs132793 polymorphism could decrease breast cancer risk and increase risks in other cancers.Overall, the results provided evidences that the single nucleotide polymorphisms in XRCC6 promoter region might play different roles in various cancers, indicating different cancers have different tumorigenesis mechanisms.0.0010857672015NA2241667677AG
rs14721891956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009NA1111962338CT
rs1472189195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009NA1111962338CT
rs149617956231678724286MITFumls:C0007134BeFreeA French and an Australian study have recently identified a rare germline functional variant in the microphthalmia-associated transcription factor (MITF) (E318K) that predisposes to familial and sporadic melanoma and to renal cell carcinoma (RCC), showing a new link between two tumour types with different risk factors and between deregulated sumoylation and cancer.0.1210857672013MITF369964940GA
rs170371021956277827123DKK2umls:C0007134BeFreeTo the authors' knowledge, this is the first report documenting that DKK3 polymorphisms are associated with RCC and that the DKK2 rs17037102 polymorphism may be a predictor for survival in patients with RCC after radical nephrectomy.0.0029099162009DKK24106924637CT,A
rs17037102195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK24106924637CT,A
rs170371021956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK24106924637CT,A
rs170371021956277827122DKK3umls:C0007134BeFreeTo the authors' knowledge, this is the first report documenting that DKK3 polymorphisms are associated with RCC and that the DKK2 rs17037102 polymorphism may be a predictor for survival in patients with RCC after radical nephrectomy.0.0031813582009DKK24106924637CT,A
rs1799793187111492068ERCC2umls:C0007134BeFreeIn individual single nucleotide polymorphism analysis, after adjustment for multiple comparisons, a significantly decreased RCC risk was observed for the heterozygous genotype of XPD Asp312Asn [odds ratio (OR) = 0.62; 95% confidence interval (CI): 0.43-0.90] and for the heterozygous and homozygous variant genotypes combined in a dominant model (OR = 0.64; 95% CI: 0.46-0.89).0.0050055062008ERCC21945364001CT
rs179986423657965729230CCR2umls:C0007134BeFreeThese data suggested that MCP-1 -2518A/G and CCR2 190G/A polymorphisms are new risk factors for RCC and could be used as prognostic markers for this malignancy.0.0005428842013CCR2346357717GA
rs180064522086884793CALB1umls:C0007134BeFreeAmong 154 newly diagnosed cases and 308 matched controls, RCC was associated with higher whole blood lead [OR = 2.0; 95% confidence interval (CI), 1.0-3.9; quartile 4 (Q4) vs. Q1, P(trend) = 0.022] and CALB1 rs1800645 (P(trend) = 0.025, minor 'T' allele frequency = 0.34).0.0002714422012CALB1890083245AT
rs1801270176345397157TP53umls:C0007134BeFreePolymorphisms of p53 Arg(72)Pro and p21 Ser(31)Arg did not show significant association with RCC.0.1503553392007CDKN1A636684194CA,T
rs18012821151191954512EXOSC4umls:C0007134BeFreeOpposite association of two PPARG variants with cancer: overrepresentation of H449H in endometrial carcinoma cases and underrepresentation of P12A in renal cell carcinoma cases.0.0002714422001PPARG312351626CG
rs18020731956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009SFRP4737907562GT
rs1802073195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009SFRP4737907562GT
rs1802074195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009SFRP4737907501CT
rs18020741956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009SFRP4737907501CT
rs18051921151191954512EXOSC4umls:C0007134BeFreeOpposite association of two PPARG variants with cancer: overrepresentation of H449H in endometrial carcinoma cases and underrepresentation of P12A in renal cell carcinoma cases.0.0002714422001PPARG312379739CG
rs18057941876850555655NLRP2umls:C0007134BeFreeUsing the homozygous wild type as the reference group, we observed a significantly increased renal cell carcinoma risk associated with the homozygous variant genotype of NBS1 (rs1805794; odds ratio, 2.13; 95% confidence interval (95% CI), 1.17-3.86).0.0005428842008NBN889978251CG
rs18057942507351455655NLRP2umls:C0007134BeFreeA number of studies have investigated the association between the NBS1 Glu185Gln (rs1805794, 8360 G>C) polymorphism and risk for urinary system cancer including bladder cancer, prostate cancer, and renal cell cancer; however, the findings are conflicting.0.0005428842014NBN889978251CG
rs20736641956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK4842374268GA
rs2073664195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK4842374268GA
rs2243250235724373565IL4umls:C0007134BeFreeTaken together, our results indicated that IL-4 rs2243250 polymorphism was associated with decreased oral cancer risk in both the homozygote contrasts and the dominant genetic model, as well as increased renal cell cancer risk in both the homozygote contrasts and the recessive genetic model.0.0082628082013IL45132673462CT
rs2267437255696442547XRCC6umls:C0007134BeFreeSensitivity analyses were also performed.The rs2267437 polymorphism was associated with a significant increase in risks of overall cancers, breast cancer, renal cell carcinoma and hepatocellular carcinoma, and it could increase the cancer risk in Asian population; the rs5751129 polymorphism could increase the cancer risk in overall cancers; the rs132770 polymorphism was associated with the increased renal cell carcinoma risk; furthermore, the rs132793 polymorphism could decrease breast cancer risk and increase risks in other cancers.Overall, the results provided evidences that the single nucleotide polymorphisms in XRCC6 promoter region might play different roles in various cancers, indicating different cancers have different tumorigenesis mechanisms.0.0010857672015XRCC6;DESI12241620695CG
rs2273535171434716790AURKAumls:C0007134BeFreeRole of the STK15 Phe31Ile polymorphism in renal cell carcinoma.0.0029099162007AURKA2056386485AT
rs2291599195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK31111968352TC
rs22915991956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK31111968352TC
rs229283224681820406938MIR146Aumls:C0007134BeFreemiR-146a rs2910164, miR-149 rs2292832, miR-196a2 rs11614913 and miR-499 rs3746444) to assess their associations with RCC risk in a two-stage case-control study (355 cases and 362 controls in discovery set, meanwhile 647 cases and 660 controls in validation set), as well as RCC survival in 311 patients.0.0026384742014GPC1;MIR149;PP145712240456086TC
rs25041061956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DAAM2639854343AG
rs2504106195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DAAM2639854343AG
rs2542222010048387119CEP85Lumls:C0007134GAD[A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.]0.0023670322012CEP85L;LOC1053779716118486684CT
rs291016424681820406938MIR146Aumls:C0007134BeFreemiR-146a rs2910164, miR-149 rs2292832, miR-196a2 rs11614913 and miR-499 rs3746444) to assess their associations with RCC risk in a two-stage case-control study (355 cases and 362 controls in discovery set, meanwhile 647 cases and 660 controls in validation set), as well as RCC survival in 311 patients.0.0026384742014LOC285628;MIR146A5160485411CG
rs3118523197531226256RXRAumls:C0007134BeFreeAcross RXRA, one haplotype located 3' of the coding sequence (rs748964, rs3118523), increased RCC risk 35% among individuals with the variant haplotype compared to those with the most common haplotype.0.0026384742009NA9134443675GA
rs3206824195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK31111964514TC
rs32068241956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK31111964514TC
rs374644424681820406938MIR146Aumls:C0007134BeFreemiR-146a rs2910164, miR-149 rs2292832, miR-196a2 rs11614913 and miR-499 rs3746444) to assess their associations with RCC risk in a two-stage case-control study (355 cases and 362 controls in discovery set, meanwhile 647 cases and 660 controls in validation set), as well as RCC survival in 311 patients.0.0026384742014MYH7B;MIR499A;MIR499B2034990448AG
rs386519031189494193091HIF1Aumls:C0007134BeFreeIn previous studies, the C1772T (P582S) or the G1790A (A588T) polymorphisms of the HIF-1alpha gene have been identified in renal cell carcinoma, head and neck and esophageal squamous cell carcinomas as well as colorectal and prostate cancers.0.036909672008NANANANANA
rs38683339523086583672BRCA1umls:C0007134BeFreeWe report the first tumor study of renal cell carcinoma in a carrier of the deleterious BRCA1 mutation-c.68_69delAG.0.0005428842013BRCA1;NBR21743124028CT-
rs419558195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK24106922935CT
rs4195581956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK24106922935CT
rs447372195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK24106932839GA
rs4473721956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK24106932839GA
rs476562321131975949SCARB1umls:C0007134GWASCATGenome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.0.2423670322011SCARB112124836304CT
rs4953345258266192034EPAS1umls:C0007134GWASCATCommon variation at 1q24.1 (ALDH9A1) is a potential risk factor for renal cancer.0.3327016862015EPAS1;LOC105374583246325462TA
rs5751129255696442547XRCC6umls:C0007134BeFreeSensitivity analyses were also performed.The rs2267437 polymorphism was associated with a significant increase in risks of overall cancers, breast cancer, renal cell carcinoma and hepatocellular carcinoma, and it could increase the cancer risk in Asian population; the rs5751129 polymorphism could increase the cancer risk in overall cancers; the rs132770 polymorphism was associated with the increased renal cell carcinoma risk; furthermore, the rs132793 polymorphism could decrease breast cancer risk and increase risks in other cancers.Overall, the results provided evidences that the single nucleotide polymorphisms in XRCC6 promoter region might play different roles in various cancers, indicating different cancers have different tumorigenesis mechanisms.0.0010857672015XRCC6;DESI12241619761CT
rs69371331956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DAAM2639832238AG
rs6937133195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DAAM2639832238AG
rs701848232097025728PTENumls:C0007134BeFreeAnother variant (rs701848) in the 3'UTR region of PTEN was associated with increased RCC risk (P = 0.014, OR = 1.45, 95%CI = 1.08-1.96, CC vs. TT); however, the association was not significant after adjusting for multiple comparisons.0.1352404712012PTEN1087966988TC
rs7105934239116363709ITPR2umls:C0007134BeFreeAfter adjusting for patient age, gender, smoking status and body mass index the AG + AA genotypes from rs7105934 (11q13) were associated with a decreased risk of renal cell carcinoma (OR 0.50, 95% CI 0.33-0.75, p = 0.001) and the AC + CC genotypes from rs1049380 (ITPR2) were associated with an increased risk (OR 1.66, 95% CI 1.28-2.16, p <0.001).0.0008143262013LOC1027242651169424973GA
rs710593421131975102724265LOC102724265umls:C0007134GWASCATGenome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.0.122011LOC1027242651169424973GA
rs7121229312422778GNASumls:C0007134BeFreeGNAS1 (Gαs) gene T393C polymorphism and renal cell carcinoma risk in a North Indian population: a case-control study.0.0005428842012GNAS2058903752CT
rs718314220100488082SSPNumls:C0007134GAD[A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.]0.0023670322012LOC1053697051226300350AG
rs718314220100483709ITPR2umls:C0007134BeFreeWe identified two common variants in linkage disequilibrium, rs718314 and rs1049380 (r(2) = 0.64, D ' = 0.84), in the inositol 1,4,5-triphosphate receptor, type 2 (ITPR2) gene on 12p11.23 as novel susceptibility loci for RCC (P = 8.89 × 10(-10) and P = 6.07 × 10(-9), respectively, in meta-analysis) with an allelic odds ratio of 1.19 [95% confidence interval (CI): 1.13-1.26] for rs718314 and 1.18 (95% CI: 1.12-1.25) for rs1049380.0.0008143262012LOC1053697051226300350AG
rs718314250536743709ITPR2umls:C0007134BeFreeA variant (rs718314) in the inositol 1,4,5-trisphosphate receptor, type 2 gene (ITPR2) was found to interact with the American/Western dietary pattern in relation to RCC risk (additive Pinteraction = 0.03).0.0008143262014LOC1053697051226300350AG
rs718314242209107515XRCC1umls:C0007134BeFreeThe 12p11.23 variant rs10771279, located 77 kb from the European-ancestry RCC marker rs718314, was associated with RCC risk in the GWAS (P = 1.2 × 10(-7)) but did not replicate (P = 0.99).0.0159391262014LOC1053697051226300350AG
rs72858496258266199839ZEB2umls:C0007134GWASCATCommon variation at 1q24.1 (ALDH9A1) is a potential risk factor for renal cancer.0.1213572092015ZEB2;LOC1053736592144452349CT
rs7396187195627786424SFRP4umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK31111967604CG
rs73961871956277823500DAAM2umls:C0007134BeFreeincluding Dickkopf 2 (DKK2) (reference SNP identification number 17037102 [rs17037102], rs419558, and rs447372), DKK3 (rs3206824, rs11022095, rs1472189, rs7396187, and rs2291599), DKK4 (rs2073664), secreted frizzled-related protein 4 (sFRP4) (rs1802073 and rs1802074), mothers against decapentaplegic homolog (SMAD) family member 7 or SMAD7 (rs12953717), and disheveled associated activator of morphogenesis 2 or DAAM2 (rs6937133 and rs2504106) using polymerase chain reaction-restriction fragment length polymorphism analysis and direct sequencing in the patients with RCC and in the healthy, age-matched control group.0.0026384742009DKK31111967604CG
rs748964197531226256RXRAumls:C0007134BeFreeAcross RXRA, one haplotype located 3' of the coding sequence (rs748964, rs3118523), increased RCC risk 35% among individuals with the variant haplotype compared to those with the most common haplotype.0.0026384742009NA9134442243CG
rs7579899211319752034EPAS1umls:C0007134GWASCATTwo correlated variants (r² = 0.99 in controls), rs11894252 (P = 1.8 × 10⁻⁸) and rs7579899 (P = 2.3 × 10⁻⁹), map to EPAS1 on 2p21, which encodes hypoxia-inducible-factor-2 alpha, a transcription factor previously implicated in RCC.0.3327016862011EPAS1;LOC105374583246310465AG
rs7579899211319752034EPAS1umls:C0007134BeFreeTwo correlated variants (r² = 0.99 in controls), rs11894252 (P = 1.8 × 10⁻⁸) and rs7579899 (P = 2.3 × 10⁻⁹), map to EPAS1 on 2p21, which encodes hypoxia-inducible-factor-2 alpha, a transcription factor previously implicated in RCC.0.3327016862011EPAS1;LOC105374583246310465AG
rs7579899211319752034EPAS1umls:C0007134GAD[Two correlated variants (rA2 = 0.99 in controls), rs11894252 (P = 1.8 A 10a>>a,) and rs7579899 (P = 2.3 A 10a>>a1), map to EPAS1 on 2p21, which encodes hypoxia-inducible-factor-2 alpha, a transcription factor previously implicated in RCC.]0.3327016862011EPAS1;LOC105374583246310465AG
rs808105925900876201266SLC39A11umls:C0007134BeFreeA ZIP11 variant, rs8081059, was significantly associated with increased risk of renal cell carcinoma (odds ratios (OR) = 1.28, 95 % confidence intervals (CI) (1.13-1.45), p = 0.049).0.0002714422015SLC39A111773072580CA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:122)
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
148063350rs10890492GArs10890492220100481.41E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
164804379rs1390473AGrs1390473242209101.60E-04NA1.54[1.23-1.92]255 African American cases; 375 African American controlsAfrican American(630)ALL(630)AFR(630)ALL(630)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerrs1390473-TMulticenter StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
185807695rs233072AGrs233072242209102.50E-04NA1.43[1.18-1.73]255 African American cases; 375 African American controlsAfrican American(630)ALL(630)AFR(630)ALL(630)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerrs233072-GMulticenter StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
215256606rs1990851AGrs1990851231841501.74E-06NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
246525391rs1867787GCrs1867787211319751.90E-07NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246526096rs10211665TCrs10211665211319751.90E-07NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246527816rs11125068AGrs11125068211319752.30E-08NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246528961rs2346417TArs2346417211319758.20E-08NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246529302rs1867783GCrs1867783211319751.30E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246533376rs11894252TCrs11894252211319759.10E-09NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246533376rs11894252TCrs11894252220100481.80E-08NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
246533552rs11684885TGrs11684885211319759.00E-09NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246534220rs1867784TCrs1867784211319756.20E-09NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246534338rs1867785AGrs1867785211319758.80E-09NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246535924rs2121266CArs2121266211319751.40E-08NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246537056rs4952818CTrs4952818211319752.80E-08NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246537604rs7579899AGrs7579899211319752.00E-09NA1.15[1.10-1.21] 3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246538794rs17034950GArs17034950211319758.20E-08NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246541176rs11689011TCrs11689011211319752.60E-08NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246546316rs2044456AGrs2044456211319754.40E-07NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246548064rs4953340CGrs4953340211319755.20E-08NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246548109rs9973653GTrs9973653211319751.60E-07NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246549040rs2034327GCrs2034327211319757.20E-07NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246549389rs2121267TCrs2121267211319752.20E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246550492rs895436GCrs895436211319756.70E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246550718rs4952819GCrs4952819211319756.80E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246552177rs4953343GCrs4953343211319753.20E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246552601rs4953345TArs4953345211319759.10E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246553966rs4952820AGrs4952820211319754.00E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246554533rs11125071CGrs11125071211319754.00E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246554646rs1868089CTrs1868089211319754.20E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246555221rs12613519AGrs12613519211319758.70E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246555263rs12613526AGrs12613526211319758.60E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246555670rs10208823TCrs10208823211319753.50E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246556633rs12712973ACrs12712973211319758.50E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246556761rs12620992GCrs12620992211319755.10E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246556824rs6706717AGrs6706717211319755.20E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG,A
246557600rs11900910CTrs11900910211319759.00E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246557644rs9679290GCrs9679290211319757.30E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246557962rs35366004GTrs35366004211319757.70E-06NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246558208rs4953346TGrs4953346211319751.40E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246558225rs4953347AGrs4953347211319751.30E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246558432rs4953348AGrs4953348211319751.40E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246558541rs6758592TCrs6758592211319752.20E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246559776rs12617313ATrs12617313211319751.90E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246560084rs11125072TArs11125072211319751.70E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246560644rs4953349TA,Grs4953349211319752.30E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246561202rs6726454AGrs6726454211319751.70E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246561309rs6726570AGrs6726570211319751.70E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246561816rs4145837GArs4145837211319751.80E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246563392rs6706003CGrs6706003211319753.40E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246564583rs4953351CArs4953351211319757.20E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246565091rs12614710TGrs12614710211319752.70E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246565522rs4953352TCrs4953352211319755.30E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246567227rs4035887AGrs4035887211319759.30E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246571310rs2346175TCrs2346175211319752.00E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246576172rs6715787CGrs6715787211319753.50E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246576488rs17035010CTrs17035010211319757.50E-05NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246576573rs17035013TCrs17035013211319751.80E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246579348rs6743087TCrs6743087211319753.50E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246579409rs6756667AGrs6756667211319759.30E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246579730rs1562451CTrs1562451211319753.50E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246580474rs1562453TCrs1562453211319756.30E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246581453rs4953358CGrs4953358211319757.50E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246581544rs7599883TArs7599883211319753.50E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246582382rs7589621GArs7589621211319753.40E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
246582891rs6712143AGrs6712143211319753.40E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246583593rs2278753GArs2278753211319756.60E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246584573rs10176396CTrs10176396211319753.20E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
246584852rs6707241CTrs6707241211319758.40E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246585888rs6740096ATrs6740096211319758.40E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246587097rs7583554TCrs7583554211319756.80E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
246589179rs4953360AGrs4953360211319756.70E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246589295rs6755594AGrs6755594211319759.00E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralA
246592006rs3768729TCrs3768729211319756.70E-04NANANA3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralT
2128404860rs3771295AGrs3771295220100481.00E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145152235rs11888238TCrs11888238231841505.03E-05NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145155731rs10185359TCrs10185359231841504.63E-04NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145169563rs7560525AGrs7560525231841502.07E-05NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145171259rs72858437TCrs72858437231841504.80E-04NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145182957rs10210063CGrs10210063231841501.70E-06NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145184316rs10192562AGrs10192562231841502.38E-06NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145193326rs10164806CTrs10164806231841501.92E-06NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145198623rs13401103GArs13401103231841506.10E-07NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145198889rs72858474GArs72858474231841504.89E-07NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145204758rs16823732GArs16823732231841501.58E-06NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145208193rs12105918TCrs12105918231841502.00E-08NA1.45[1.20-1.75] 2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145208336rs12105521GA,Trs12105521231841507.28E-07NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145209916rs72858496CTrs72858496231841505.76E-07NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145213638rs731108GCrs731108231841501.34E-06NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145216048rs13389578TCrs13389578231841503.58E-06NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2145216132rs13401515ATrs13401515231841502.43E-06NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
32561556rs17620999AGrs17620999231841502.11E-05NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
357473750rs10510793GArs10510793220100484.49E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
3194328524rs789997AGrs789997231841506.44E-06NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
532000483rs10054504TCrs10054504231841508.00E-07NA1.37[1.19-1.58] 2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
685777822rs7765284CArs7765284231841509.37E-07NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
6118807847rs25422CTrs25422220100485.00E-06NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
7129670412rs4507692TCrs4507692220100482.10E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
8128889371rs6470588ACrs35252396242206995.00E-11(rs35252396-CG, rs6470588-C, rs6470589-G)1.27[1.18-1.37] 1,505 European ancestry cases; 67,725 European ancestry controlsEuropean(69230)ALL(69230)EUR(69230)ALL(69230)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tNAPVT1
1031388250rs7080444CTrs7080444220100488.36E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1031415106rs793108CTrs793108220100481.29E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1031418463rs1340991AGrs1340991220100486.45E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1052036514rs10508925GArs10508925220100482.78E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1169234494rs4980785CTrs4980785220100482.00E-06NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1169239741rs7105934GArs7105934211319758.00E-14NA1.45[1.32-1.61]3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralG
1169239741rs7105934GArs7105934220100487.80E-14NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
11113864109rs897685CTrs897685220100484.32E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
11127659737rs371808590GCAGrs6590279220100483.72E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
11127659737rs6590279GArs6590279220100483.72E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1226453283rs718314AGrs718314220100489.00E-10NA1.19[1.13-1.26]894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1226489544rs1049380GTrs1049380220100486.07E-09NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1226530543rs10771279TCrs10771279242209107.60E-05NA1.54[1.23-1.89]255 African American cases; 375 African American controlsAfrican American(630)ALL(630)AFR(630)ALL(630)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerrs10771279-TMulticenter StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
12125320850rs4765623CTrs4765623211319753.00E-08NA1.15[1.09-1.20] 3,772 European descent cases; 8,505 European descent controlsEuropean(12277)ALL(12277)EUR(12277)ALL(12277)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., IntramuralC
12129853660rs11060283CTrs11060283220100488.21E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1452884355rs10143866TCrs10143866220100485.19E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
1657341599rs1645893AGrs1645893242209109.50E-06NA1.49[1.25-1.79]255 African American cases; 375 African American controlsAfrican American(630)ALL(630)AFR(630)ALL(630)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerrs1645893-TMulticenter StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1763549488rs3923086ACrs3923086220100481.66E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2043871071rs6017525AGrs6017525220100482.74E-04NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2117758842rs1449522TCrs1449522220100482.05E-05NANANA894 European ancestry cases; 1,516 European ancestry controlsEuropean(2410)ALL(2410)EUR(2410)ALL(2410)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2139257377rs2836034AGrs2836034231841504.56E-05NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
2230221120rs11549795CTrs11549795231841501.45E-05NANANA2,215 European ancestry cases; 8,566 European ancestry controlsEuropean(10781)ALL(10781)EUR(10781)ALL(10781)Renal cell carcinomaHPOID:0005584Renal cell carcinomaDOID:4450renal cell carcinomaD002292Carcinoma, Renal CellEFOID:0000681renal cell carcinomaRenal Cell cancerNAMeta-AnalysisResearch Support, Non-U.S. Gov'tResearch Support, N.I.H., Intramural
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 98
Disease renal cell carcinoma
Case(Waiting for update.)