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PedAM

Pediatric Disease Annotations & Medicines



   renal cell carcinoma
  

Disease ID 28
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:153)
C0040053  |  thrombus  |  46
C0022658  |  renal disease  |  13
C0022661  |  end-stage renal disease  |  12
C0019562  |  lindau disease  |  11
C0028754  |  obesity  |  10
C0040053  |  thrombosis  |  8
C0022658  |  kidney disease  |  8
C0022661  |  chronic kidney disease  |  7
C0019562  |  von hippel-lindau disease  |  7
C0153676  |  lung metastases  |  7
C0019562  |  hippel-lindau disease  |  7
C0153676  |  lung metastasis  |  6
C0020538  |  hypertension  |  6
C0153676  |  pulmonary metastasis  |  6
C0346010  |  birt-hogg-dube syndrome  |  5
C0032285  |  pneumonitis  |  5
C0011847  |  diabetes  |  5
C0220650  |  brain metastases  |  5
C0024623  |  gastric cancer  |  4
C0041341  |  tuberous sclerosis  |  4
C0220650  |  brain metastasis  |  4
C0008325  |  cholecystitis  |  4
C0836924  |  thrombocytosis  |  3
C0153676  |  pulmonary metastases  |  3
C0019562  |  von hippel lindau disease  |  3
C0023827  |  liposarcoma  |  3
C0011849  |  diabetes mellitus  |  3
C0278678  |  metastatic renal cell carcinoma  |  3
C0036202  |  sarcoid  |  3
C0029463  |  osteosarcoma  |  3
C0018801  |  heart failure  |  3
C0020676  |  hypothyroidism  |  3
C0267841  |  acalculous cholecystitis  |  3
C0279702  |  clear cell renal cell carcinoma  |  2
C0022116  |  ischemia  |  2
C0007112  |  prostatic adenocarcinoma  |  2
C0740457  |  kidney cancer  |  2
C0085413  |  autosomal dominant polycystic kidney disease  |  2
C0206734  |  hemangioblastoma  |  2
C0686619  |  lymph node metastases  |  2
C0948265  |  metabolic syndrome  |  2
C0036202  |  sarcoidosis  |  2
C0007134  |  renal carcinoma  |  2
C0034150  |  purpura  |  2
C0494165  |  hepatic metastases  |  2
C0025202  |  melanoma  |  2
C0206654  |  leiomyomatosis  |  2
C0007138  |  urothelial carcinoma  |  2
C0751571  |  urological cancers  |  2
C0751571  |  urological cancer  |  2
C0022679  |  cystic kidney  |  2
C0740457  |  renal cancer  |  2
C0442874  |  neuropathy  |  2
C0494165  |  liver metastases  |  2
C0085413  |  autosomal dominant polycystic kidney  |  2
C0024299  |  lymphoma  |  2
C0854178  |  adrenal metastases  |  2
C0001430  |  adenoma  |  1
C0699790  |  colon carcinoma  |  1
C0019204  |  hepatocellular carcinoma  |  1
C0014868  |  esophagitis  |  1
C0009402  |  colorectal carcinoma  |  1
C0022354  |  cholestatic jaundice  |  1
C0037054  |  sickle-cell trait  |  1
C0751690  |  malignant peripheral nerve sheath tumor  |  1
C0027708  |  nephroblastoma  |  1
C0007114  |  skin cancer  |  1
C0040034  |  thrombocytopenia  |  1
C0020437  |  hypercalcemia  |  1
C0030805  |  bullous pemphigoid  |  1
C0242231  |  coronary artery stenosis  |  1
C0025202  |  melanomas  |  1
C0024143  |  lupus nephritis  |  1
C1691228  |  renal cystic disease  |  1
C0027726  |  nephrotic syndrome  |  1
C0153687  |  skin metastasis  |  1
C0235974  |  carcinoma of the pancreas  |  1
C0346255  |  renal oncocytoma  |  1
C0042384  |  vasculitis  |  1
C0001418  |  adenocarcinoma  |  1
C0023434  |  chronic lymphocytic leukaemia  |  1
C1561644  |  chronic kidney disease (ckd)  |  1
C1266045  |  metanephric adenoma  |  1
C0007115  |  thyroid ca  |  1
C0023801  |  lipomatosis  |  1
C0017525  |  giant cell tumors  |  1
C0034931  |  reflex sympathetic dystrophy  |  1
C0085652  |  pyoderma gangrenosum  |  1
C0018802  |  congestive heart failure  |  1
C0030805  |  pemphigoid  |  1
C0346976  |  pancreatic metastasis  |  1
C0003873  |  rheumatoid arthritis  |  1
C0007113  |  rectal carcinoma  |  1
C1565489  |  renal insufficiency  |  1
C0020459  |  hyperinsulinism  |  1
C0007137  |  squamous cell carcinomas  |  1
C0241961  |  renal angiomyolipoma  |  1
C0206633  |  angiomyolipoma  |  1
C0034065  |  pulmonary embolism  |  1
C0221348  |  yellow nail syndrome  |  1
C0035078  |  renal failure  |  1
C0002871  |  anemia  |  1
C0017525  |  giant cell tumor  |  1
C0376545  |  hematological malignancies  |  1
C0004030  |  aspergillosis  |  1
C0005684  |  bladder cancer  |  1
C0023530  |  leukopenia  |  1
C0149925  |  small cell carcinoma  |  1
C0007137  |  squamous cell carcinoma  |  1
C0271355  |  sixth nerve palsy  |  1
C0003864  |  arthritis  |  1
C0018916  |  hemangioma  |  1
C0001815  |  myelofibrosis  |  1
C1306837  |  papillary renal cell carcinoma  |  1
C0278883  |  metastatic melanoma  |  1
C0006142  |  breast cancer  |  1
C0008370  |  cholestasis  |  1
C0027708  |  nephroma  |  1
C0018552  |  hamartoma  |  1
C0019829  |  hodgkin lymphoma  |  1
C0024291  |  hemophagocytic syndrome  |  1
C0033117  |  priapism  |  1
C1266042  |  chromophobe renal cell carcinoma  |  1
C0021831  |  bowel disease  |  1
C0020538  |  high blood pressure  |  1
C0002871  |  anaemia  |  1
C0043117  |  immune thrombocytopenic purpura  |  1
C0029132  |  optic neuropathy  |  1
C0024305  |  non-hodgkin lymphoma  |  1
C0021390  |  inflammatory bowel disease  |  1
C0032285  |  pneumonia  |  1
C0023903  |  liver tumor  |  1
C0019621  |  langerhans cell histiocytosis  |  1
C0270922  |  demyelinating neuropathy  |  1
C0155773  |  portal vein thrombosis  |  1
C0024236  |  lymphedema  |  1
C0022661  |  chronic renal failure  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0026896  |  myasthenia gravis  |  1
C0043117  |  idiopathic thrombocytopenic purpura  |  1
C0549473  |  thyroid carcinoma  |  1
C0019618  |  histiocytosis  |  1
C0022661  |  chronic renal disease  |  1
C0023448  |  lymphocytic leukaemia  |  1
C0007642  |  cellulitis  |  1
C0035328  |  retinal vein occlusion  |  1
C0019562  |  von hippel-lindau syndrome  |  1
C0023267  |  leiomyoma  |  1
C0206681  |  clear cell adenocarcinoma  |  1
C0021933  |  intussusception  |  1
C0154841  |  central retinal vein occlusion  |  1
C0041341  |  tuberous sclerosis complex  |  1
C0494165  |  liver metastasis  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:125)
SLC2A1  |  6513  |  CTD_human
IL6  |  3569  |  CTD_human
EEF2  |  1938  |  CTD_human
SOD2  |  6648  |  CTD_human
BAP1  |  8314  |  CTD_human
PIK3CA  |  5290  |  CTD_human
POMC  |  5443  |  CTD_human
LMAN2L  |  81562  |  CTD_human
APRT  |  353  |  CTD_human
TP53  |  7157  |  CTD_human
PVALB  |  5816  |  CTD_human
MET  |  4233  |  CLINVAR;CTD_human
RYR1  |  6261  |  CTD_human
CTSD  |  1509  |  CTD_human
PRAME  |  23532  |  CTD_human
KEAP1  |  9817  |  CTD_human
IL13  |  3596  |  CTD_human
OGG1  |  4968  |  CTD_human
HNF1B  |  6928  |  CTD_human
IL6R  |  3570  |  CTD_human
ZEB2  |  9839  |  GWASCAT
RELA  |  5970  |  CTD_human
TET2  |  54790  |  CTD_human
ERBB2  |  2064  |  CTD_human
SPTBN4  |  57731  |  CTD_human
CRADD  |  8738  |  CTD_human
PTGS2  |  5743  |  CTD_human
HNF1A  |  6927  |  CTD_human
PDXDC1  |  23042  |  CTD_human
TNFSF10  |  8743  |  CTD_human
NF2  |  4771  |  CTD_human
AHNAK  |  79026  |  CTD_human
NDRG1  |  10397  |  CTD_human
PBRM1  |  55193  |  CTD_human
PTEN  |  5728  |  CTD_human
BCHE  |  590  |  CTD_human
PRCC  |  5546  |  CTD_human
IFNA2  |  3440  |  CTD_human
CRYAB  |  1410  |  CTD_human
MUC4  |  4585  |  CTD_human
TSC1  |  7248  |  CTD_human
SHANK1  |  50944  |  CTD_human
FLT1  |  2321  |  CTD_human
HSPD1  |  3329  |  CTD_human
CARD11  |  84433  |  CTD_human
CUL7  |  9820  |  CTD_human
MLLT10  |  8028  |  CTD_human
MITF  |  4286  |  CTD_human
HARS  |  3035  |  CTD_human
TGM2  |  7052  |  CTD_human
BIRC5  |  332  |  CTD_human
GSTP1  |  2950  |  CTD_human
CRABP1  |  1381  |  CTD_human
SYNE2  |  23224  |  CTD_human
EPAS1  |  2034  |  CTD_human;GWASCAT
NLRP12  |  91662  |  CTD_human
FAM111B  |  374393  |  CTD_human
MTOR  |  2475  |  CTD_human
FLCN  |  201163  |  CTD_human
L1CAM  |  3897  |  CTD_human
PDHB  |  5162  |  CTD_human
ACHE  |  43  |  CTD_human
TFE3  |  7030  |  CTD_human
KRT8  |  3856  |  CTD_human
KRT7  |  3855  |  CTD_human
GSTM1  |  2944  |  CTD_human
PEBP1  |  5037  |  CTD_human
KRT32  |  3882  |  CTD_human
GRB7  |  2886  |  CTD_human
BTG3  |  10950  |  CTD_human
GJB1  |  2705  |  CTD_human
M6PR  |  4074  |  CTD_human
PGK1  |  5230  |  CTD_human
PAK1  |  5058  |  CTD_human
YIPF3  |  25844  |  CTD_human
FMN2  |  56776  |  CTD_human
CSMD3  |  114788  |  CTD_human
VHL  |  7428  |  CTD_human
HSPA9  |  3313  |  CTD_human
APAF1  |  317  |  CTD_human
CNN2  |  1265  |  CTD_human
KCNMA1  |  3778  |  CTD_human
SFRP2  |  6423  |  CTD_human
RNF139  |  11236  |  CTD_human
HSPB1  |  3315  |  CTD_human
GSTT1  |  2952  |  CTD_human
CTSB  |  1508  |  CTD_human
AKAP13  |  11214  |  CTD_human
CASP2  |  835  |  CTD_human
SETD2  |  29072  |  CTD_human
ANXA4  |  307  |  CTD_human
ALK  |  238  |  CTD_human
LRRK2  |  120892  |  CTD_human
LRP1B  |  53353  |  CTD_human
FPGT  |  8790  |  CTD_human
DAPK1  |  1612  |  CTD_human
KDM5C  |  8242  |  CTD_human
ALAD  |  210  |  CTD_human
PDZD2  |  23037  |  GWASCAT
ZNF536  |  9745  |  CTD_human
SLC5A3  |  6526  |  CTD_human
PNKD  |  25953  |  CTD_human
ALDH1A1  |  216  |  CTD_human
CAPG  |  822  |  CTD_human
VMO1  |  284013  |  CTD_human
AP5M1  |  55745  |  CTD_human
IL4R  |  3566  |  CTD_human
SCARB1  |  949  |  CTD_human;GWASCAT
FAAH2  |  158584  |  CTD_human
ZNF804A  |  91752  |  CTD_human
TAGLN2  |  8407  |  CTD_human
CPQ  |  10404  |  CTD_human
UNC5C  |  8633  |  CTD_human
ZNF765  |  91661  |  CTD_human
NAV3  |  89795  |  CTD_human
BIRC7  |  79444  |  CTD_human
ASB15  |  142685  |  CTD_human
DNHD1  |  144132  |  CTD_human
PIDD1  |  55367  |  CTD_human
ACY1  |  95  |  CTD_human
OR4C13  |  283092  |  CTD_human
DIRC2  |  84925  |  CTD_human
MSGN1  |  343930  |  CTD_human
RPL14  |  9045  |  CTD_human
LDHB  |  3945  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:8)
2034  |  EPAS1  |  infer
390218  |  IFITM9P  |  infer
949  |  SCARB1  |  infer
8082  |  SSPN  |  infer
3105  |  HLA-A  |  infer
6390  |  SDHB  |  infer
7421  |  VDR  |  infer
7428  |  VHL  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:1711)
100302650  |  BRE-AS1  |  DISEASES
100302650  |  BRE-AS1  |  DISEASES
613126  |  CYP51A1-AS1  |  DISEASES
613126  |  CYP51A1-AS1  |  DISEASES
10344  |  CCL26  |  DISEASES
10344  |  CCL26  |  DISEASES
928  |  CD9  |  DISEASES
928  |  CD9  |  DISEASES
4830  |  NME1  |  DISEASES
4830  |  NME1  |  DISEASES
6591  |  SNAI2  |  DISEASES
6591  |  SNAI2  |  DISEASES
1015  |  CDH17  |  DISEASES
1015  |  CDH17  |  DISEASES
340533  |  KIAA2022  |  DISEASES
340533  |  KIAA2022  |  DISEASES
602  |  BCL3  |  DISEASES
602  |  BCL3  |  DISEASES
22846  |  VASH1  |  DISEASES
22846  |  VASH1  |  DISEASES
3861  |  KRT14  |  DISEASES
3861  |  KRT14  |  DISEASES
54474  |  KRT20  |  DISEASES
54474  |  KRT20  |  DISEASES
3566  |  IL4R  |  DISEASES
3566  |  IL4R  |  DISEASES
9817  |  KEAP1  |  DISEASES
9817  |  KEAP1  |  DISEASES
7145  |  TNS1  |  DISEASES
7145  |  TNS1  |  DISEASES
6793  |  STK10  |  DISEASES
6793  |  STK10  |  DISEASES
771  |  CA12  |  DISEASES
771  |  CA12  |  DISEASES
83641  |  FAM107B  |  DISEASES
83641  |  FAM107B  |  DISEASES
10777  |  ARPP21  |  DISEASES
10777  |  ARPP21  |  DISEASES
3902  |  LAG3  |  DISEASES
3902  |  LAG3  |  DISEASES
2099  |  ESR1  |  DISEASES
2099  |  ESR1  |  DISEASES
7414  |  VCL  |  DISEASES
7414  |  VCL  |  DISEASES
5594  |  MAPK1  |  DISEASES
5594  |  MAPK1  |  DISEASES
5816  |  PVALB  |  DISEASES
5816  |  PVALB  |  DISEASES
7380  |  UPK3A  |  DISEASES
7380  |  UPK3A  |  DISEASES
9978  |  RBX1  |  DISEASES
9978  |  RBX1  |  DISEASES
3002  |  GZMB  |  DISEASES
3002  |  GZMB  |  DISEASES
1113  |  CHGA  |  DISEASES
1113  |  CHGA  |  DISEASES
4792  |  NFKBIA  |  DISEASES
4792  |  NFKBIA  |  DISEASES
6790  |  AURKA  |  DISEASES
6790  |  AURKA  |  DISEASES
2937  |  GSS  |  DISEASES
79444  |  BIRC7  |  DISEASES
79444  |  BIRC7  |  DISEASES
54941  |  RNF125  |  DISEASES
7076  |  TIMP1  |  DISEASES
7076  |  TIMP1  |  DISEASES
4313  |  MMP2  |  DISEASES
4313  |  MMP2  |  DISEASES
5713  |  PSMD7  |  DISEASES
5713  |  PSMD7  |  DISEASES
7249  |  TSC2  |  DISEASES
7249  |  TSC2  |  DISEASES
7038  |  TG  |  DISEASES
7038  |  TG  |  DISEASES
6422  |  SFRP1  |  DISEASES
6422  |  SFRP1  |  DISEASES
27121  |  DKK4  |  DISEASES
27121  |  DKK4  |  DISEASES
8797  |  TNFRSF10A  |  DISEASES
8797  |  TNFRSF10A  |  DISEASES
7733  |  ZNF180  |  DISEASES
7733  |  ZNF180  |  DISEASES
7040  |  TGFB1  |  DISEASES
7040  |  TGFB1  |  DISEASES
973  |  CD79A  |  DISEASES
973  |  CD79A  |  DISEASES
1048  |  CEACAM5  |  DISEASES
1048  |  CEACAM5  |  DISEASES
2057  |  EPOR  |  DISEASES
2057  |  EPOR  |  DISEASES
59284  |  CACNG7  |  DISEASES
59284  |  CACNG7  |  DISEASES
3082  |  HGF  |  DISEASES
3082  |  HGF  |  DISEASES
3696  |  ITGB8  |  DISEASES
3696  |  ITGB8  |  DISEASES
858  |  CAV2  |  DISEASES
858  |  CAV2  |  DISEASES
1577  |  CYP3A5  |  DISEASES
1577  |  CYP3A5  |  DISEASES
5054  |  SERPINE1  |  DISEASES
5054  |  SERPINE1  |  DISEASES
7431  |  VIM  |  DISEASES
7431  |  VIM  |  DISEASES
56521  |  DNAJC12  |  DISEASES
56521  |  DNAJC12  |  DISEASES
1440  |  CSF3  |  DISEASES
1440  |  CSF3  |  DISEASES
6198  |  RPS6KB1  |  DISEASES
6198  |  RPS6KB1  |  DISEASES
5216  |  PFN1  |  DISEASES
5216  |  PFN1  |  DISEASES
6347  |  CCL2  |  DISEASES
6347  |  CCL2  |  DISEASES
6928  |  HNF1B  |  DISEASES
6928  |  HNF1B  |  DISEASES
3558  |  IL2  |  DISEASES
3558  |  IL2  |  DISEASES
3732  |  CD82  |  DISEASES
3732  |  CD82  |  DISEASES
595  |  CCND1  |  DISEASES
595  |  CCND1  |  DISEASES
79080  |  CCDC86  |  DISEASES
79080  |  CCDC86  |  DISEASES
4254  |  KITLG  |  DISEASES
4254  |  KITLG  |  DISEASES
5829  |  PXN  |  DISEASES
5829  |  PXN  |  DISEASES
969  |  CD69  |  DISEASES
969  |  CD69  |  DISEASES
2735  |  GLI1  |  DISEASES
2735  |  GLI1  |  DISEASES
1027  |  CDKN1B  |  DISEASES
1027  |  CDKN1B  |  DISEASES
11211  |  FZD10  |  DISEASES
11211  |  FZD10  |  DISEASES
55801  |  IL26  |  DISEASES
55801  |  IL26  |  DISEASES
3458  |  IFNG  |  DISEASES
3458  |  IFNG  |  DISEASES
2597  |  GAPDH  |  DISEASES
2597  |  GAPDH  |  DISEASES
84519  |  ACRBP  |  DISEASES
84519  |  ACRBP  |  DISEASES
2026  |  ENO2  |  DISEASES
2026  |  ENO2  |  DISEASES
2729  |  GCLC  |  DISEASES
2729  |  GCLC  |  DISEASES
51522  |  TMEM14C  |  DISEASES
51522  |  TMEM14C  |  DISEASES
1432  |  MAPK14  |  DISEASES
1432  |  MAPK14  |  DISEASES
7942  |  TFEB  |  DISEASES
7942  |  TFEB  |  DISEASES
6908  |  TBP  |  DISEASES
6908  |  TBP  |  DISEASES
3910  |  LAMA4  |  DISEASES
3910  |  LAMA4  |  DISEASES
4015  |  LOX  |  DISEASES
4015  |  LOX  |  DISEASES
26167  |  PCDHB5  |  DISEASES
26167  |  PCDHB5  |  DISEASES
3565  |  IL4  |  DISEASES
3565  |  IL4  |  DISEASES
4292  |  MLH1  |  DISEASES
4292  |  MLH1  |  DISEASES
4436  |  MSH2  |  DISEASES
4436  |  MSH2  |  DISEASES
374291  |  NDUFS7  |  DISEASES
374291  |  NDUFS7  |  DISEASES
4999  |  ORC2  |  DISEASES
4999  |  ORC2  |  DISEASES
84634  |  KISS1R  |  DISEASES
84634  |  KISS1R  |  DISEASES
2956  |  MSH6  |  DISEASES
2956  |  MSH6  |  DISEASES
10459  |  MAD2L2  |  DISEASES
10459  |  MAD2L2  |  DISEASES
6402  |  SELL  |  DISEASES
6402  |  SELL  |  DISEASES
7276  |  TTR  |  DISEASES
7276  |  TTR  |  DISEASES
9519  |  TBPL1  |  DISEASES
9519  |  TBPL1  |  DISEASES
6943  |  TCF21  |  DISEASES
6943  |  TCF21  |  DISEASES
9429  |  ABCG2  |  DISEASES
9429  |  ABCG2  |  DISEASES
8405  |  SPOP  |  DISEASES
8405  |  SPOP  |  DISEASES
8743  |  TNFSF10  |  DISEASES
8743  |  TNFSF10  |  DISEASES
2322  |  FLT3  |  DISEASES
2322  |  FLT3  |  DISEASES
7291  |  TWIST1  |  DISEASES
7291  |  TWIST1  |  DISEASES
6615  |  SNAI1  |  DISEASES
6615  |  SNAI1  |  DISEASES
1026  |  CDKN1A  |  DISEASES
1026  |  CDKN1A  |  DISEASES
4502  |  MT2A  |  DISEASES
4502  |  MT2A  |  DISEASES
9271  |  PIWIL1  |  DISEASES
9271  |  PIWIL1  |  DISEASES
3659  |  IRF1  |  DISEASES
3659  |  IRF1  |  DISEASES
970  |  CD70  |  DISEASES
970  |  CD70  |  DISEASES
1236  |  CCR7  |  DISEASES
1236  |  CCR7  |  DISEASES
59269  |  HIVEP3  |  DISEASES
59269  |  HIVEP3  |  DISEASES
9143  |  SYNGR3  |  DISEASES
9143  |  SYNGR3  |  DISEASES
3315  |  HSPB1  |  DISEASES
3315  |  HSPB1  |  DISEASES
2678  |  GGT1  |  DISEASES
2678  |  GGT1  |  DISEASES
2952  |  GSTT1  |  DISEASES
2952  |  GSTT1  |  DISEASES
54567  |  DLL4  |  DISEASES
54567  |  DLL4  |  DISEASES
968  |  CD68  |  DISEASES
968  |  CD68  |  DISEASES
112399  |  EGLN3  |  DISEASES
112399  |  EGLN3  |  DISEASES
239  |  ALOX12  |  DISEASES
239  |  ALOX12  |  DISEASES
79977  |  GRHL2  |  DISEASES
79977  |  GRHL2  |  DISEASES
5894  |  RAF1  |  DISEASES
5894  |  RAF1  |  DISEASES
1890  |  TYMP  |  DISEASES
1890  |  TYMP  |  DISEASES
3852  |  KRT5  |  DISEASES
3852  |  KRT5  |  DISEASES
25796  |  PGLS  |  DISEASES
25796  |  PGLS  |  DISEASES
2056  |  EPO  |  DISEASES
2056  |  EPO  |  DISEASES
140628  |  GATA5  |  DISEASES
140628  |  GATA5  |  DISEASES
10343  |  PKDREJ  |  DISEASES
10343  |  PKDREJ  |  DISEASES
9113  |  LATS1  |  DISEASES
9476  |  NAPSA  |  DISEASES
9476  |  NAPSA  |  DISEASES
8572  |  PDLIM4  |  DISEASES
8572  |  PDLIM4  |  DISEASES
3958  |  LGALS3  |  DISEASES
3958  |  LGALS3  |  DISEASES
23135  |  KDM6B  |  DISEASES
23135  |  KDM6B  |  DISEASES
182  |  JAG1  |  DISEASES
182  |  JAG1  |  DISEASES
1401  |  CRP  |  DISEASES
1401  |  CRP  |  DISEASES
55643  |  BTBD2  |  DISEASES
55643  |  BTBD2  |  DISEASES
3845  |  KRAS  |  DISEASES
3845  |  KRAS  |  DISEASES
759  |  CA1  |  DISEASES
759  |  CA1  |  DISEASES
56154  |  TEX15  |  DISEASES
891  |  CCNB1  |  DISEASES
891  |  CCNB1  |  DISEASES
7428  |  VHL  |  DISEASES
7428  |  VHL  |  DISEASES
2922  |  GRP  |  DISEASES
2922  |  GRP  |  DISEASES
2346  |  FOLH1  |  DISEASES
2346  |  FOLH1  |  DISEASES
5156  |  PDGFRA  |  DISEASES
5156  |  PDGFRA  |  DISEASES
29923  |  HILPDA  |  DISEASES
29923  |  HILPDA  |  DISEASES
1019  |  CDK4  |  DISEASES
1019  |  CDK4  |  DISEASES
3569  |  IL6  |  DISEASES
3569  |  IL6  |  DISEASES
153090  |  DAB2IP  |  DISEASES
153090  |  DAB2IP  |  DISEASES
1318  |  SLC31A2  |  DISEASES
1318  |  SLC31A2  |  DISEASES
4856  |  NOV  |  DISEASES
4856  |  NOV  |  DISEASES
5460  |  POU5F1  |  DISEASES
5460  |  POU5F1  |  DISEASES
4316  |  MMP7  |  DISEASES
4316  |  MMP7  |  DISEASES
7057  |  THBS1  |  DISEASES
7057  |  THBS1  |  DISEASES
56924  |  PAK6  |  DISEASES
56924  |  PAK6  |  DISEASES
1545  |  CYP1B1  |  DISEASES
1545  |  CYP1B1  |  DISEASES
51163  |  DBR1  |  DISEASES
9360  |  PPIG  |  DISEASES
9360  |  PPIG  |  DISEASES
84925  |  DIRC2  |  DISEASES
84925  |  DIRC2  |  DISEASES
4069  |  LYZ  |  DISEASES
4069  |  LYZ  |  DISEASES
23398  |  PPWD1  |  DISEASES
23398  |  PPWD1  |  DISEASES
5037  |  PEBP1  |  DISEASES
5037  |  PEBP1  |  DISEASES
999  |  CDH1  |  DISEASES
999  |  CDH1  |  DISEASES
5159  |  PDGFRB  |  DISEASES
5159  |  PDGFRB  |  DISEASES
10681  |  GNB5  |  DISEASES
10681  |  GNB5  |  DISEASES
2324  |  FLT4  |  DISEASES
2324  |  FLT4  |  DISEASES
57045  |  TWSG1  |  DISEASES
57045  |  TWSG1  |  DISEASES
81671  |  VMP1  |  DISEASES
81671  |  VMP1  |  DISEASES
2201  |  FBN2  |  DISEASES
2201  |  FBN2  |  DISEASES
4969  |  OGN  |  DISEASES
4969  |  OGN  |  DISEASES
7077  |  TIMP2  |  DISEASES
7077  |  TIMP2  |  DISEASES
1871  |  E2F3  |  DISEASES
1871  |  E2F3  |  DISEASES
5595  |  MAPK3  |  DISEASES
5595  |  MAPK3  |  DISEASES
1326  |  MAP3K8  |  DISEASES
1326  |  MAP3K8  |  DISEASES
6598  |  SMARCB1  |  DISEASES
6598  |  SMARCB1  |  DISEASES
6855  |  SYP  |  DISEASES
6855  |  SYP  |  DISEASES
2033  |  EP300  |  DISEASES
2033  |  EP300  |  DISEASES
7299  |  TYR  |  DISEASES
3552  |  IL1A  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
3553  |  IL1B  |  DISEASES
29842  |  TFCP2L1  |  DISEASES
29842  |  TFCP2L1  |  DISEASES
2034  |  EPAS1  |  DISEASES
2034  |  EPAS1  |  DISEASES
4072  |  EPCAM  |  DISEASES
4072  |  EPCAM  |  DISEASES
4722  |  NDUFS3  |  DISEASES
4722  |  NDUFS3  |  DISEASES
3574  |  IL7  |  DISEASES
3574  |  IL7  |  DISEASES
6801  |  STRN  |  DISEASES
6801  |  STRN  |  DISEASES
3791  |  KDR  |  DISEASES
3791  |  KDR  |  DISEASES
5290  |  PIK3CA  |  DISEASES
5290  |  PIK3CA  |  DISEASES
4162  |  MCAM  |  DISEASES
4162  |  MCAM  |  DISEASES
80303  |  EFHD1  |  DISEASES
80303  |  EFHD1  |  DISEASES
10382  |  TUBB4A  |  DISEASES
941  |  CD80  |  DISEASES
941  |  CD80  |  DISEASES
57600  |  FNIP2  |  DISEASES
57600  |  FNIP2  |  DISEASES
59067  |  IL21  |  DISEASES
59067  |  IL21  |  DISEASES
2247  |  FGF2  |  DISEASES
2247  |  FGF2  |  DISEASES
27338  |  UBE2S  |  DISEASES
1356  |  CP  |  DISEASES
1356  |  CP  |  DISEASES
6774  |  STAT3  |  DISEASES
6774  |  STAT3  |  DISEASES
50509  |  COL5A3  |  DISEASES
50509  |  COL5A3  |  DISEASES
3383  |  ICAM1  |  DISEASES
3383  |  ICAM1  |  DISEASES
53371  |  NUP54  |  DISEASES
53371  |  NUP54  |  DISEASES
306  |  ANXA3  |  DISEASES
6389  |  SDHA  |  DISEASES
6389  |  SDHA  |  DISEASES
1004  |  CDH6  |  DISEASES
1004  |  CDH6  |  DISEASES
8614  |  STC2  |  DISEASES
8614  |  STC2  |  DISEASES
2028  |  ENPEP  |  DISEASES
2028  |  ENPEP  |  DISEASES
51176  |  LEF1  |  DISEASES
51176  |  LEF1  |  DISEASES
1950  |  EGF  |  DISEASES
1950  |  EGF  |  DISEASES
793  |  CALB1  |  DISEASES
793  |  CALB1  |  DISEASES
22797  |  TFEC  |  DISEASES
22797  |  TFEC  |  DISEASES
27074  |  LAMP3  |  DISEASES
27074  |  LAMP3  |  DISEASES
4885  |  NPTX2  |  DISEASES
4885  |  NPTX2  |  DISEASES
5243  |  ABCB1  |  DISEASES
5243  |  ABCB1  |  DISEASES
29999  |  FSCN3  |  DISEASES
29999  |  FSCN3  |  DISEASES
38  |  ACAT1  |  DISEASES
38  |  ACAT1  |  DISEASES
5395  |  PMS2  |  DISEASES
5395  |  PMS2  |  DISEASES
10180  |  RBM6  |  DISEASES
10180  |  RBM6  |  DISEASES
7078  |  TIMP3  |  DISEASES
939  |  CD27  |  DISEASES
939  |  CD27  |  DISEASES
6636  |  SNRPF  |  DISEASES
6636  |  SNRPF  |  DISEASES
1017  |  CDK2  |  DISEASES
1017  |  CDK2  |  DISEASES
2065  |  ERBB3  |  DISEASES
2065  |  ERBB3  |  DISEASES
5925  |  RB1  |  DISEASES
5925  |  RB1  |  DISEASES
3480  |  IGF1R  |  DISEASES
3480  |  IGF1R  |  DISEASES
51458  |  RHCG  |  DISEASES
51458  |  RHCG  |  DISEASES
1009  |  CDH11  |  DISEASES
81631  |  MAP1LC3B  |  DISEASES
81631  |  MAP1LC3B  |  DISEASES
28987  |  NOB1  |  DISEASES
28987  |  NOB1  |  DISEASES
85464  |  SSH2  |  DISEASES
85464  |  SSH2  |  DISEASES
1213  |  CLTC  |  DISEASES
1213  |  CLTC  |  DISEASES
1000  |  CDH2  |  DISEASES
1000  |  CDH2  |  DISEASES
7157  |  TP53  |  DISEASES
7157  |  TP53  |  DISEASES
94015  |  TTYH2  |  DISEASES
94015  |  TTYH2  |  DISEASES
57332  |  CBX8  |  DISEASES
57332  |  CBX8  |  DISEASES
6398  |  SECTM1  |  DISEASES
6398  |  SECTM1  |  DISEASES
2064  |  ERBB2  |  DISEASES
2064  |  ERBB2  |  DISEASES
3487  |  IGFBP4  |  DISEASES
3487  |  IGFBP4  |  DISEASES
207  |  AKT1  |  DISEASES
207  |  AKT1  |  DISEASES
5546  |  PRCC  |  DISEASES
5546  |  PRCC  |  DISEASES
6282  |  S100A11  |  DISEASES
6282  |  S100A11  |  DISEASES
1513  |  CTSK  |  DISEASES
1513  |  CTSK  |  DISEASES
10637  |  LEFTY1  |  DISEASES
10637  |  LEFTY1  |  DISEASES
5972  |  REN  |  DISEASES
5972  |  REN  |  DISEASES
388  |  RHOB  |  DISEASES
388  |  RHOB  |  DISEASES
83607  |  AMMECR1L  |  DISEASES
83607  |  AMMECR1L  |  DISEASES
26018  |  LRIG1  |  DISEASES
26018  |  LRIG1  |  DISEASES
10330  |  CNPY2  |  DISEASES
10330  |  CNPY2  |  DISEASES
185  |  AGTR1  |  DISEASES
185  |  AGTR1  |  DISEASES
6502  |  SKP2  |  DISEASES
6502  |  SKP2  |  DISEASES
3001  |  GZMA  |  DISEASES
3001  |  GZMA  |  DISEASES
78991  |  PCYOX1L  |  DISEASES
78991  |  PCYOX1L  |  DISEASES
353219  |  KAAG1  |  DISEASES
353219  |  KAAG1  |  DISEASES
222663  |  SCUBE3  |  DISEASES
1956  |  EGFR  |  DISEASES
1956  |  EGFR  |  DISEASES
2041  |  EPHA1  |  DISEASES
2041  |  EPHA1  |  DISEASES
4841  |  NONO  |  DISEASES
4841  |  NONO  |  DISEASES
8795  |  TNFRSF10B  |  DISEASES
8795  |  TNFRSF10B  |  DISEASES
123  |  PLIN2  |  DISEASES
123  |  PLIN2  |  DISEASES
1030  |  CDKN2B  |  DISEASES
1030  |  CDKN2B  |  DISEASES
3439  |  IFNA1  |  DISEASES
3439  |  IFNA1  |  DISEASES
3934  |  LCN2  |  DISEASES
3934  |  LCN2  |  DISEASES
4851  |  NOTCH1  |  DISEASES
4851  |  NOTCH1  |  DISEASES
5058  |  PAK1  |  DISEASES
5058  |  PAK1  |  DISEASES
3145  |  HMBS  |  DISEASES
3145  |  HMBS  |  DISEASES
90952  |  ESAM  |  DISEASES
7424  |  VEGFC  |  DISEASES
7424  |  VEGFC  |  DISEASES
5805  |  PTS  |  DISEASES
5805  |  PTS  |  DISEASES
127124  |  ATP6V1G3  |  DISEASES
127124  |  ATP6V1G3  |  DISEASES
202559  |  KHDRBS2  |  DISEASES
202559  |  KHDRBS2  |  DISEASES
5281  |  PIGF  |  DISEASES
5281  |  PIGF  |  DISEASES
120224  |  TMEM45B  |  DISEASES
120224  |  TMEM45B  |  DISEASES
4249  |  MGAT5  |  DISEASES
5741  |  PTH  |  DISEASES
5741  |  PTH  |  DISEASES
2321  |  FLT1  |  DISEASES
2321  |  FLT1  |  DISEASES
10413  |  YAP1  |  DISEASES
10413  |  YAP1  |  DISEASES
89780  |  WNT3A  |  DISEASES
89780  |  WNT3A  |  DISEASES
201163  |  FLCN  |  DISEASES
201163  |  FLCN  |  DISEASES
27123  |  DKK2  |  DISEASES
27123  |  DKK2  |  DISEASES
760  |  CA2  |  DISEASES
760  |  CA2  |  DISEASES
1436  |  CSF1R  |  DISEASES
1436  |  CSF1R  |  DISEASES
7411  |  VBP1  |  DISEASES
7411  |  VBP1  |  DISEASES
11197  |  WIF1  |  DISEASES
11197  |  WIF1  |  DISEASES
9073  |  CLDN8  |  DISEASES
9073  |  CLDN8  |  DISEASES
23420  |  NOMO1  |  DISEASES
5468  |  PPARG  |  DISEASES
5468  |  PPARG  |  DISEASES
146456  |  TMED6  |  DISEASES
146456  |  TMED6  |  DISEASES
3815  |  KIT  |  DISEASES
3815  |  KIT  |  DISEASES
5291  |  PIK3CB  |  DISEASES
5291  |  PIK3CB  |  DISEASES
9669  |  EIF5B  |  DISEASES
9669  |  EIF5B  |  DISEASES
909  |  CD1A  |  DISEASES
909  |  CD1A  |  DISEASES
27005  |  USP21  |  DISEASES
27005  |  USP21  |  DISEASES
5909  |  RAP1GAP  |  DISEASES
5909  |  RAP1GAP  |  DISEASES
112950  |  MED8  |  DISEASES
112950  |  MED8  |  DISEASES
1636  |  ACE  |  DISEASES
1636  |  ACE  |  DISEASES
30815  |  ST6GALNAC6  |  DISEASES
30815  |  ST6GALNAC6  |  DISEASES
9437  |  NCR1  |  DISEASES
9437  |  NCR1  |  DISEASES
486  |  FXYD2  |  DISEASES
486  |  FXYD2  |  DISEASES
6271  |  S100A1  |  DISEASES
6271  |  S100A1  |  DISEASES
9794  |  MAML1  |  DISEASES
9794  |  MAML1  |  DISEASES
3856  |  KRT8  |  DISEASES
3856  |  KRT8  |  DISEASES
6777  |  STAT5B  |  DISEASES
6777  |  STAT5B  |  DISEASES
3678  |  ITGA5  |  DISEASES
3678  |  ITGA5  |  DISEASES
140807  |  KRT72  |  DISEASES
140807  |  KRT72  |  DISEASES
58191  |  CXCL16  |  DISEASES
58191  |  CXCL16  |  DISEASES
10630  |  PDPN  |  DISEASES
10630  |  PDPN  |  DISEASES
7412  |  VCAM1  |  DISEASES
7412  |  VCAM1  |  DISEASES
2215  |  FCGR3B  |  DISEASES
2215  |  FCGR3B  |  DISEASES
79762  |  C1orf115  |  DISEASES
79762  |  C1orf115  |  DISEASES
5937  |  RBMS1  |  DISEASES
5966  |  REL  |  DISEASES
5966  |  REL  |  DISEASES
27306  |  HPGDS  |  DISEASES
27306  |  HPGDS  |  DISEASES
4286  |  MITF  |  DISEASES
4286  |  MITF  |  DISEASES
213  |  ALB  |  DISEASES
213  |  ALB  |  DISEASES
6374  |  CXCL5  |  DISEASES
6374  |  CXCL5  |  DISEASES
64866  |  CDCP1  |  DISEASES
64866  |  CDCP1  |  DISEASES
83597  |  RTP3  |  DISEASES
83597  |  RTP3  |  DISEASES
79442  |  LRRC2  |  DISEASES
79442  |  LRRC2  |  DISEASES
4486  |  MST1R  |  DISEASES
4486  |  MST1R  |  DISEASES
308  |  ANXA5  |  DISEASES
308  |  ANXA5  |  DISEASES
3600  |  IL15  |  DISEASES
3600  |  IL15  |  DISEASES
3673  |  ITGA2  |  DISEASES
4724  |  NDUFS4  |  DISEASES
4724  |  NDUFS4  |  DISEASES
10915  |  TCERG1  |  DISEASES
10915  |  TCERG1  |  DISEASES
134288  |  TMEM174  |  DISEASES
134288  |  TMEM174  |  DISEASES
9607  |  CARTPT  |  DISEASES
9607  |  CARTPT  |  DISEASES
1437  |  CSF2  |  DISEASES
1437  |  CSF2  |  DISEASES
55568  |  GALNT10  |  DISEASES
55568  |  GALNT10  |  DISEASES
6469  |  SHH  |  DISEASES
6469  |  SHH  |  DISEASES
2020  |  EN2  |  DISEASES
2020  |  EN2  |  DISEASES
1672  |  DEFB1  |  DISEASES
1672  |  DEFB1  |  DISEASES
157753  |  TMEM74  |  DISEASES
157753  |  TMEM74  |  DISEASES
220296  |  HEPACAM  |  DISEASES
220296  |  HEPACAM  |  DISEASES
114088  |  TRIM9  |  DISEASES
114088  |  TRIM9  |  DISEASES
120939  |  TMEM52B  |  DISEASES
120939  |  TMEM52B  |  DISEASES
7248  |  TSC1  |  DISEASES
7248  |  TSC1  |  DISEASES
57447  |  NDRG2  |  DISEASES
57447  |  NDRG2  |  DISEASES
9317  |  PTER  |  DISEASES
9317  |  PTER  |  DISEASES
4108  |  MAGEA9  |  DISEASES
4108  |  MAGEA9  |  DISEASES
143689  |  PIWIL4  |  DISEASES
143689  |  PIWIL4  |  DISEASES
55662  |  HIF1AN  |  DISEASES
55662  |  HIF1AN  |  DISEASES
3611  |  ILK  |  DISEASES
3611  |  ILK  |  DISEASES
7551  |  ZNF3  |  DISEASES
7551  |  ZNF3  |  DISEASES
1014  |  CDH16  |  DISEASES
1014  |  CDH16  |  DISEASES
4837  |  NNMT  |  DISEASES
4837  |  NNMT  |  DISEASES
89927  |  C16orf45  |  DISEASES
290  |  ANPEP  |  DISEASES
290  |  ANPEP  |  DISEASES
22974  |  TPX2  |  DISEASES
22974  |  TPX2  |  DISEASES
29123  |  ANKRD11  |  DISEASES
29123  |  ANKRD11  |  DISEASES
121268  |  RHEBL1  |  DISEASES
121268  |  RHEBL1  |  DISEASES
558  |  AXL  |  DISEASES
558  |  AXL  |  DISEASES
10653  |  SPINT2  |  DISEASES
10653  |  SPINT2  |  DISEASES
3816  |  KLK1  |  DISEASES
51129  |  ANGPTL4  |  DISEASES
51129  |  ANGPTL4  |  DISEASES
332  |  BIRC5  |  DISEASES
332  |  BIRC5  |  DISEASES
7083  |  TK1  |  DISEASES
7083  |  TK1  |  DISEASES
8772  |  FADD  |  DISEASES
8772  |  FADD  |  DISEASES
84168  |  ANTXR1  |  DISEASES
84168  |  ANTXR1  |  DISEASES
81603  |  TRIM8  |  DISEASES
81603  |  TRIM8  |  DISEASES
79058  |  ASPSCR1  |  DISEASES
79058  |  ASPSCR1  |  DISEASES
5604  |  MAP2K1  |  DISEASES
5604  |  MAP2K1  |  DISEASES
9839  |  ZEB2  |  DISEASES
9839  |  ZEB2  |  DISEASES
598  |  BCL2L1  |  DISEASES
598  |  BCL2L1  |  DISEASES
3479  |  IGF1  |  DISEASES
3479  |  IGF1  |  DISEASES
5734  |  PTGER4  |  DISEASES
5734  |  PTGER4  |  DISEASES
6203  |  RPS9  |  DISEASES
6203  |  RPS9  |  DISEASES
3308  |  HSPA4  |  DISEASES
3308  |  HSPA4  |  DISEASES
3688  |  ITGB1  |  DISEASES
3688  |  ITGB1  |  DISEASES
10960  |  LMAN2  |  DISEASES
10960  |  LMAN2  |  DISEASES
8988  |  HSPB3  |  DISEASES
8988  |  HSPB3  |  DISEASES
1493  |  CTLA4  |  DISEASES
1493  |  CTLA4  |  DISEASES
11236  |  RNF139  |  DISEASES
11236  |  RNF139  |  DISEASES
171558  |  PTCRA  |  DISEASES
171558  |  PTCRA  |  DISEASES
28991  |  COMMD5  |  DISEASES
28991  |  COMMD5  |  DISEASES
3596  |  IL13  |  DISEASES
3596  |  IL13  |  DISEASES
84342  |  COG8  |  DISEASES
84342  |  COG8  |  DISEASES
3627  |  CXCL10  |  DISEASES
3627  |  CXCL10  |  DISEASES
2353  |  FOS  |  DISEASES
2353  |  FOS  |  DISEASES
7369  |  UMOD  |  DISEASES
7369  |  UMOD  |  DISEASES
4968  |  OGG1  |  DISEASES
4968  |  OGG1  |  DISEASES
8493  |  PPM1D  |  DISEASES
8493  |  PPM1D  |  DISEASES
6373  |  CXCL11  |  DISEASES
6373  |  CXCL11  |  DISEASES
112398  |  EGLN2  |  DISEASES
112398  |  EGLN2  |  DISEASES
9451  |  EIF2AK3  |  DISEASES
9451  |  EIF2AK3  |  DISEASES
57521  |  RPTOR  |  DISEASES
57521  |  RPTOR  |  DISEASES
794  |  CALB2  |  DISEASES
794  |  CALB2  |  DISEASES
152189  |  CMTM8  |  DISEASES
152189  |  CMTM8  |  DISEASES
54205  |  CYCS  |  DISEASES
54205  |  CYCS  |  DISEASES
27087  |  B3GAT1  |  DISEASES
27087  |  B3GAT1  |  DISEASES
5986  |  RFNG  |  DISEASES
5986  |  RFNG  |  DISEASES
4323  |  MMP14  |  DISEASES
4323  |  MMP14  |  DISEASES
991  |  CDC20  |  DISEASES
991  |  CDC20  |  DISEASES
2147  |  F2  |  DISEASES
2147  |  F2  |  DISEASES
5340  |  PLG  |  DISEASES
5340  |  PLG  |  DISEASES
7015  |  TERT  |  DISEASES
7015  |  TERT  |  DISEASES
3265  |  HRAS  |  DISEASES
3265  |  HRAS  |  DISEASES
6868  |  ADAM17  |  DISEASES
947  |  CD34  |  DISEASES
947  |  CD34  |  DISEASES
5708  |  PSMD2  |  DISEASES
9092  |  SART1  |  DISEASES
9092  |  SART1  |  DISEASES
9416  |  DDX23  |  DISEASES
9416  |  DDX23  |  DISEASES
5598  |  MAPK7  |  DISEASES
836  |  CASP3  |  DISEASES
836  |  CASP3  |  DISEASES
1163  |  CKS1B  |  DISEASES
1163  |  CKS1B  |  DISEASES
358  |  AQP1  |  DISEASES
358  |  AQP1  |  DISEASES
2944  |  GSTM1  |  DISEASES
2944  |  GSTM1  |  DISEASES
27239  |  GPR162  |  DISEASES
27239  |  GPR162  |  DISEASES
80227  |  PAAF1  |  DISEASES
2250  |  FGF5  |  DISEASES
2250  |  FGF5  |  DISEASES
55167  |  MSL2  |  DISEASES
55167  |  MSL2  |  DISEASES
84868  |  HAVCR2  |  DISEASES
84868  |  HAVCR2  |  DISEASES
3069  |  HDLBP  |  DISEASES
3069  |  HDLBP  |  DISEASES
5098  |  PCDHGC3  |  DISEASES
5098  |  PCDHGC3  |  DISEASES
54961  |  SSH3  |  DISEASES
54961  |  SSH3  |  DISEASES
55279  |  ZNF654  |  DISEASES
55279  |  ZNF654  |  DISEASES
64759  |  TNS3  |  DISEASES
64759  |  TNS3  |  DISEASES
56667  |  MUC13  |  DISEASES
8837  |  CFLAR  |  DISEASES
8837  |  CFLAR  |  DISEASES
3172  |  HNF4A  |  DISEASES
3172  |  HNF4A  |  DISEASES
3817  |  KLK2  |  DISEASES
8877  |  SPHK1  |  DISEASES
29882  |  ANAPC2  |  DISEASES
29882  |  ANAPC2  |  DISEASES
7030  |  TFE3  |  DISEASES
7030  |  TFE3  |  DISEASES
354  |  KLK3  |  DISEASES
354  |  KLK3  |  DISEASES
79929  |  MAP6D1  |  DISEASES
79929  |  MAP6D1  |  DISEASES
285  |  ANGPT2  |  DISEASES
285  |  ANGPT2  |  DISEASES
27122  |  DKK3  |  DISEASES
27122  |  DKK3  |  DISEASES
5430  |  POLR2A  |  DISEASES
5430  |  POLR2A  |  DISEASES
1191  |  CLU  |  DISEASES
1191  |  CLU  |  DISEASES
7298  |  TYMS  |  DISEASES
7298  |  TYMS  |  DISEASES
165721  |  DNAJB8  |  DISEASES
165721  |  DNAJB8  |  DISEASES
8560  |  DEGS1  |  DISEASES
8560  |  DEGS1  |  DISEASES
22998  |  LIMCH1  |  DISEASES
22998  |  LIMCH1  |  DISEASES
4233  |  MET  |  DISEASES
4233  |  MET  |  DISEASES
8939  |  FUBP3  |  DISEASES
8939  |  FUBP3  |  DISEASES
4684  |  NCAM1  |  DISEASES
4684  |  NCAM1  |  DISEASES
55076  |  TMEM45A  |  DISEASES
55076  |  TMEM45A  |  DISEASES
58492  |  ZNF77  |  DISEASES
58492  |  ZNF77  |  DISEASES
3579  |  CXCR2  |  DISEASES
3579  |  CXCR2  |  DISEASES
8834  |  TMEM11  |  DISEASES
8834  |  TMEM11  |  DISEASES
80381  |  CD276  |  DISEASES
80381  |  CD276  |  DISEASES
2146  |  EZH2  |  DISEASES
2146  |  EZH2  |  DISEASES
5315  |  PKM  |  DISEASES
5315  |  PKM  |  DISEASES
124961  |  ZFP3  |  DISEASES
124961  |  ZFP3  |  DISEASES
8289  |  ARID1A  |  DISEASES
8289  |  ARID1A  |  DISEASES
91445  |  RNF185  |  DISEASES
91445  |  RNF185  |  DISEASES
50628  |  GEMIN4  |  DISEASES
50628  |  GEMIN4  |  DISEASES
3992  |  FADS1  |  DISEASES
3992  |  FADS1  |  DISEASES
93129  |  ORAI3  |  DISEASES
93129  |  ORAI3  |  DISEASES
3039  |  HBA1  |  DISEASES
3039  |  HBA1  |  DISEASES
64089  |  SNX16  |  DISEASES
64089  |  SNX16  |  DISEASES
4312  |  MMP1  |  DISEASES
4312  |  MMP1  |  DISEASES
2274  |  FHL2  |  DISEASES
923  |  CD6  |  DISEASES
923  |  CD6  |  DISEASES
27036  |  SIGLEC7  |  DISEASES
27036  |  SIGLEC7  |  DISEASES
57125  |  PLXDC1  |  DISEASES
57125  |  PLXDC1  |  DISEASES
8408  |  ULK1  |  DISEASES
8408  |  ULK1  |  DISEASES
29841  |  GRHL1  |  DISEASES
29841  |  GRHL1  |  DISEASES
60485  |  SAV1  |  DISEASES
60485  |  SAV1  |  DISEASES
2932  |  GSK3B  |  DISEASES
2932  |  GSK3B  |  DISEASES
5241  |  PGR  |  DISEASES
5241  |  PGR  |  DISEASES
2300  |  FOXL1  |  DISEASES
2300  |  FOXL1  |  DISEASES
8454  |  CUL1  |  DISEASES
8454  |  CUL1  |  DISEASES
10693  |  CCT6B  |  DISEASES
10693  |  CCT6B  |  DISEASES
84193  |  SETD3  |  DISEASES
84193  |  SETD3  |  DISEASES
1435  |  CSF1  |  DISEASES
1435  |  CSF1  |  DISEASES
1789  |  DNMT3B  |  DISEASES
256949  |  KANK3  |  DISEASES
256949  |  KANK3  |  DISEASES
5454  |  POU3F2  |  DISEASES
5454  |  POU3F2  |  DISEASES
4105  |  MAGEA6  |  DISEASES
4105  |  MAGEA6  |  DISEASES
3855  |  KRT7  |  DISEASES
3855  |  KRT7  |  DISEASES
440822  |  PIWIL3  |  DISEASES
440822  |  PIWIL3  |  DISEASES
842  |  CASP9  |  DISEASES
842  |  CASP9  |  DISEASES
5155  |  PDGFB  |  DISEASES
5155  |  PDGFB  |  DISEASES
4496  |  MT1H  |  DISEASES
4496  |  MT1H  |  DISEASES
4707  |  NDUFB1  |  DISEASES
4707  |  NDUFB1  |  DISEASES
30834  |  ZNRD1  |  DISEASES
30834  |  ZNRD1  |  DISEASES
7490  |  WT1  |  DISEASES
7490  |  WT1  |  DISEASES
6401  |  SELE  |  DISEASES
6401  |  SELE  |  DISEASES
796  |  CALCA  |  DISEASES
796  |  CALCA  |  DISEASES
2621  |  GAS6  |  DISEASES
2621  |  GAS6  |  DISEASES
942  |  CD86  |  DISEASES
942  |  CD86  |  DISEASES
283208  |  P4HA3  |  DISEASES
283208  |  P4HA3  |  DISEASES
5915  |  RARB  |  DISEASES
5915  |  RARB  |  DISEASES
1485  |  CTAG1B  |  DISEASES
1485  |  CTAG1B  |  DISEASES
682  |  BSG  |  DISEASES
682  |  BSG  |  DISEASES
146223  |  CMTM4  |  DISEASES
146223  |  CMTM4  |  DISEASES
151888  |  BTLA  |  DISEASES
151888  |  BTLA  |  DISEASES
5133  |  PDCD1  |  DISEASES
5133  |  PDCD1  |  DISEASES
353322  |  ANKRD37  |  DISEASES
353322  |  ANKRD37  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
157567  |  ANKRD46  |  DISEASES
157567  |  ANKRD46  |  DISEASES
283  |  ANG  |  DISEASES
9547  |  CXCL14  |  DISEASES
9547  |  CXCL14  |  DISEASES
9166  |  EBAG9  |  DISEASES
9166  |  EBAG9  |  DISEASES
3932  |  LCK  |  DISEASES
3932  |  LCK  |  DISEASES
1576  |  CYP3A4  |  DISEASES
1576  |  CYP3A4  |  DISEASES
135138  |  PACRG  |  DISEASES
135138  |  PACRG  |  DISEASES
3091  |  HIF1A  |  DISEASES
3091  |  HIF1A  |  DISEASES
23462  |  HEY1  |  DISEASES
23462  |  HEY1  |  DISEASES
318  |  NUDT2  |  DISEASES
2246  |  FGF1  |  DISEASES
23583  |  SMUG1  |  DISEASES
23583  |  SMUG1  |  DISEASES
7430  |  EZR  |  DISEASES
6175  |  RPLP0  |  DISEASES
6175  |  RPLP0  |  DISEASES
3266  |  ERAS  |  DISEASES
3266  |  ERAS  |  DISEASES
857  |  CAV1  |  DISEASES
857  |  CAV1  |  DISEASES
5329  |  PLAUR  |  DISEASES
4697  |  NDUFA4  |  DISEASES
4697  |  NDUFA4  |  DISEASES
1978  |  EIF4EBP1  |  DISEASES
1978  |  EIF4EBP1  |  DISEASES
2810  |  SFN  |  DISEASES
23136  |  EPB41L3  |  DISEASES
23136  |  EPB41L3  |  DISEASES
5747  |  PTK2  |  DISEASES
5747  |  PTK2  |  DISEASES
6776  |  STAT5A  |  DISEASES
6776  |  STAT5A  |  DISEASES
85360  |  SYDE1  |  DISEASES
85360  |  SYDE1  |  DISEASES
4089  |  SMAD4  |  DISEASES
4089  |  SMAD4  |  DISEASES
84335  |  AKT1S1  |  DISEASES
84335  |  AKT1S1  |  DISEASES
2804  |  GOLGB1  |  DISEASES
2272  |  FHIT  |  DISEASES
2272  |  FHIT  |  DISEASES
2066  |  ERBB4  |  DISEASES
3716  |  JAK1  |  DISEASES
3716  |  JAK1  |  DISEASES
9474  |  ATG5  |  DISEASES
9474  |  ATG5  |  DISEASES
23405  |  DICER1  |  DISEASES
23405  |  DICER1  |  DISEASES
1499  |  CTNNB1  |  DISEASES
1499  |  CTNNB1  |  DISEASES
84940  |  CORO6  |  DISEASES
84940  |  CORO6  |  DISEASES
10950  |  BTG3  |  DISEASES
4771  |  NF2  |  DISEASES
4771  |  NF2  |  DISEASES
162966  |  ZNF600  |  DISEASES
162966  |  ZNF600  |  DISEASES
26762  |  HAVCR1  |  DISEASES
26762  |  HAVCR1  |  DISEASES
9232  |  PTTG1  |  DISEASES
9232  |  PTTG1  |  DISEASES
7171  |  TPM4  |  DISEASES
7171  |  TPM4  |  DISEASES
1869  |  E2F1  |  DISEASES
1869  |  E2F1  |  DISEASES
7005  |  TEAD3  |  DISEASES
7005  |  TEAD3  |  DISEASES
10168  |  ZNF197  |  DISEASES
302  |  ANXA2  |  DISEASES
302  |  ANXA2  |  DISEASES
6275  |  S100A4  |  DISEASES
2534  |  FYN  |  DISEASES
5325  |  PLAGL1  |  DISEASES
5325  |  PLAGL1  |  DISEASES
223  |  ALDH9A1  |  DISEASES
223  |  ALDH9A1  |  DISEASES
2335  |  FN1  |  DISEASES
2335  |  FN1  |  DISEASES
7080  |  NKX2-1  |  DISEASES
7080  |  NKX2-1  |  DISEASES
131920  |  TMEM207  |  DISEASES
131920  |  TMEM207  |  DISEASES
728  |  C5AR1  |  DISEASES
728  |  C5AR1  |  DISEASES
80781  |  COL18A1  |  DISEASES
80781  |  COL18A1  |  DISEASES
331  |  XIAP  |  DISEASES
331  |  XIAP  |  DISEASES
161291  |  TMEM30B  |  DISEASES
161291  |  TMEM30B  |  DISEASES
5979  |  RET  |  DISEASES
5979  |  RET  |  DISEASES
355  |  FAS  |  DISEASES
355  |  FAS  |  DISEASES
26503  |  SLC17A5  |  DISEASES
26503  |  SLC17A5  |  DISEASES
5265  |  SERPINA1  |  DISEASES
3240  |  HP  |  DISEASES
3240  |  HP  |  DISEASES
140732  |  SUN5  |  DISEASES
140732  |  SUN5  |  DISEASES
7068  |  THRB  |  DISEASES
7068  |  THRB  |  DISEASES
6288  |  SAA1  |  DISEASES
6288  |  SAA1  |  DISEASES
4100  |  MAGEA1  |  DISEASES
4100  |  MAGEA1  |  DISEASES
5725  |  PTBP1  |  DISEASES
11186  |  RASSF1  |  DISEASES
11186  |  RASSF1  |  DISEASES
10445  |  MCRS1  |  DISEASES
10445  |  MCRS1  |  DISEASES
6421  |  SFPQ  |  DISEASES
6421  |  SFPQ  |  DISEASES
56882  |  CDC42SE1  |  DISEASES
56882  |  CDC42SE1  |  DISEASES
440738  |  MAP1LC3C  |  DISEASES
253260  |  RICTOR  |  DISEASES
253260  |  RICTOR  |  DISEASES
60  |  ACTB  |  DISEASES
60  |  ACTB  |  DISEASES
728378  |  POTEF  |  DISEASES
728378  |  POTEF  |  DISEASES
54437  |  SEMA5B  |  DISEASES
54437  |  SEMA5B  |  DISEASES
286319  |  TUSC1  |  DISEASES
286319  |  TUSC1  |  DISEASES
6597  |  SMARCA4  |  DISEASES
6597  |  SMARCA4  |  DISEASES
1612  |  DAPK1  |  DISEASES
1612  |  DAPK1  |  DISEASES
79366  |  HMGN5  |  DISEASES
79366  |  HMGN5  |  DISEASES
23567  |  ZNF346  |  DISEASES
23567  |  ZNF346  |  DISEASES
6714  |  SRC  |  DISEASES
6714  |  SRC  |  DISEASES
1969  |  EPHA2  |  DISEASES
1969  |  EPHA2  |  DISEASES
841  |  CASP8  |  DISEASES
841  |  CASP8  |  DISEASES
405  |  ARNT  |  DISEASES
405  |  ARNT  |  DISEASES
26057  |  ANKRD17  |  DISEASES
26057  |  ANKRD17  |  DISEASES
2526  |  FUT4  |  DISEASES
2526  |  FUT4  |  DISEASES
9332  |  CD163  |  DISEASES
9332  |  CD163  |  DISEASES
2547  |  XRCC6  |  DISEASES
2547  |  XRCC6  |  DISEASES
1786  |  DNMT1  |  DISEASES
1786  |  DNMT1  |  DISEASES
26020  |  LRP10  |  DISEASES
126014  |  OSCAR  |  DISEASES
126014  |  OSCAR  |  DISEASES
55959  |  SULF2  |  DISEASES
113146  |  AHNAK2  |  DISEASES
113146  |  AHNAK2  |  DISEASES
3135  |  HLA-G  |  DISEASES
3135  |  HLA-G  |  DISEASES
1366  |  CLDN7  |  DISEASES
1366  |  CLDN7  |  DISEASES
5599  |  MAPK8  |  DISEASES
5599  |  MAPK8  |  DISEASES
8828  |  NRP2  |  DISEASES
8828  |  NRP2  |  DISEASES
4311  |  MME  |  DISEASES
4311  |  MME  |  DISEASES
1803  |  DPP4  |  DISEASES
1803  |  DPP4  |  DISEASES
1565  |  CYP2D6  |  DISEASES
1565  |  CYP2D6  |  DISEASES
54106  |  TLR9  |  DISEASES
54106  |  TLR9  |  DISEASES
11170  |  FAM107A  |  DISEASES
11170  |  FAM107A  |  DISEASES
57111  |  RAB25  |  DISEASES
57111  |  RAB25  |  DISEASES
6772  |  STAT1  |  DISEASES
6772  |  STAT1  |  DISEASES
6935  |  ZEB1  |  DISEASES
6935  |  ZEB1  |  DISEASES
7150  |  TOP1  |  DISEASES
7150  |  TOP1  |  DISEASES
2475  |  MTOR  |  DISEASES
2475  |  MTOR  |  DISEASES
2882  |  GPX7  |  DISEASES
2882  |  GPX7  |  DISEASES
919  |  CD247  |  DISEASES
919  |  CD247  |  DISEASES
800  |  CALD1  |  DISEASES
800  |  CALD1  |  DISEASES
2705  |  GJB1  |  DISEASES
2705  |  GJB1  |  DISEASES
4283  |  CXCL9  |  DISEASES
4283  |  CXCL9  |  DISEASES
9824  |  ARHGAP11A  |  DISEASES
9824  |  ARHGAP11A  |  DISEASES
3880  |  KRT19  |  DISEASES
3880  |  KRT19  |  DISEASES
8678  |  BECN1  |  DISEASES
8678  |  BECN1  |  DISEASES
5891  |  MOK  |  DISEASES
5891  |  MOK  |  DISEASES
7052  |  TGM2  |  DISEASES
7052  |  TGM2  |  DISEASES
2271  |  FH  |  DISEASES
2271  |  FH  |  DISEASES
2786  |  GNG4  |  DISEASES
2786  |  GNG4  |  DISEASES
54583  |  EGLN1  |  DISEASES
54583  |  EGLN1  |  DISEASES
142  |  PARP1  |  DISEASES
142  |  PARP1  |  DISEASES
3814  |  KISS1  |  DISEASES
3814  |  KISS1  |  DISEASES
7432  |  VIP  |  DISEASES
7432  |  VIP  |  DISEASES
5788  |  PTPRC  |  DISEASES
5788  |  PTPRC  |  DISEASES
79577  |  CDC73  |  DISEASES
79577  |  CDC73  |  DISEASES
5743  |  PTGS2  |  DISEASES
5743  |  PTGS2  |  DISEASES
116496  |  FAM129A  |  DISEASES
27101  |  CACYBP  |  DISEASES
27101  |  CACYBP  |  DISEASES
356  |  FASLG  |  DISEASES
356  |  FASLG  |  DISEASES
2214  |  FCGR3A  |  DISEASES
2214  |  FCGR3A  |  DISEASES
6391  |  SDHC  |  DISEASES
6391  |  SDHC  |  DISEASES
911  |  CD1C  |  DISEASES
911  |  CD1C  |  DISEASES
1382  |  CRABP2  |  DISEASES
1382  |  CRABP2  |  DISEASES
4582  |  MUC1  |  DISEASES
4582  |  MUC1  |  DISEASES
2173  |  FABP7  |  DISEASES
2173  |  FABP7  |  DISEASES
7170  |  TPM3  |  DISEASES
7170  |  TPM3  |  DISEASES
664  |  BNIP3  |  DISEASES
664  |  BNIP3  |  DISEASES
6276  |  S100A5  |  DISEASES
56647  |  BCCIP  |  DISEASES
56647  |  BCCIP  |  DISEASES
4170  |  MCL1  |  DISEASES
4170  |  MCL1  |  DISEASES
23632  |  CA14  |  DISEASES
2209  |  FCGR1A  |  DISEASES
2209  |  FCGR1A  |  DISEASES
58528  |  RRAGD  |  DISEASES
58528  |  RRAGD  |  DISEASES
79679  |  VTCN1  |  DISEASES
79679  |  VTCN1  |  DISEASES
965  |  CD58  |  DISEASES
965  |  CD58  |  DISEASES
148281  |  SYT6  |  DISEASES
148281  |  SYT6  |  DISEASES
7162  |  TPBG  |  DISEASES
7162  |  TPBG  |  DISEASES
25950  |  RWDD3  |  DISEASES
6319  |  SCD  |  DISEASES
6319  |  SCD  |  DISEASES
2258  |  FGF13  |  DISEASES
2258  |  FGF13  |  DISEASES
959  |  CD40LG  |  DISEASES
959  |  CD40LG  |  DISEASES
204962  |  SLC44A5  |  DISEASES
204962  |  SLC44A5  |  DISEASES
163782  |  KANK4  |  DISEASES
163782  |  KANK4  |  DISEASES
1791  |  DNTT  |  DISEASES
1791  |  DNTT  |  DISEASES
3725  |  JUN  |  DISEASES
3725  |  JUN  |  DISEASES
199964  |  TMEM61  |  DISEASES
199964  |  TMEM61  |  DISEASES
84871  |  AGBL4  |  DISEASES
284541  |  CYP4A22  |  DISEASES
284541  |  CYP4A22  |  DISEASES
5728  |  PTEN  |  DISEASES
5728  |  PTEN  |  DISEASES
154796  |  AMOT  |  DISEASES
154796  |  AMOT  |  DISEASES
7422  |  VEGFA  |  DISEASES
7422  |  VEGFA  |  DISEASES
958  |  CD40  |  DISEASES
958  |  CD40  |  DISEASES
4318  |  MMP9  |  DISEASES
4318  |  MMP9  |  DISEASES
4904  |  YBX1  |  DISEASES
4904  |  YBX1  |  DISEASES
89891  |  WDR34  |  DISEASES
89891  |  WDR34  |  DISEASES
5328  |  PLAU  |  DISEASES
5328  |  PLAU  |  DISEASES
10487  |  CAP1  |  DISEASES
170384  |  FUT11  |  DISEASES
170384  |  FUT11  |  DISEASES
896  |  CCND3  |  DISEASES
896  |  CCND3  |  DISEASES
2022  |  ENG  |  DISEASES
2022  |  ENG  |  DISEASES
23051  |  ZHX3  |  DISEASES
23051  |  ZHX3  |  DISEASES
2516  |  NR5A1  |  DISEASES
2516  |  NR5A1  |  DISEASES
2833  |  CXCR3  |  DISEASES
2833  |  CXCR3  |  DISEASES
2934  |  GSN  |  DISEASES
2934  |  GSN  |  DISEASES
1104  |  RCC1  |  DISEASES
1104  |  RCC1  |  DISEASES
7185  |  TRAF1  |  DISEASES
7185  |  TRAF1  |  DISEASES
143162  |  FRMPD2  |  DISEASES
143162  |  FRMPD2  |  DISEASES
3561  |  IL2RG  |  DISEASES
3561  |  IL2RG  |  DISEASES
6676  |  SPAG4  |  DISEASES
6676  |  SPAG4  |  DISEASES
53828  |  FXYD4  |  DISEASES
53828  |  FXYD4  |  DISEASES
7295  |  TXN  |  DISEASES
7295  |  TXN  |  DISEASES
367  |  AR  |  DISEASES
367  |  AR  |  DISEASES
5698  |  PSMB9  |  DISEASES
5698  |  PSMB9  |  DISEASES
5696  |  PSMB8  |  DISEASES
5696  |  PSMB8  |  DISEASES
7046  |  TGFBR1  |  DISEASES
3014  |  H2AFX  |  DISEASES
643008  |  SMIM5  |  DISEASES
643008  |  SMIM5  |  DISEASES
8242  |  KDM5C  |  DISEASES
8242  |  KDM5C  |  DISEASES
81569  |  ACTL8  |  DISEASES
81569  |  ACTL8  |  DISEASES
55920  |  RCC2  |  DISEASES
55920  |  RCC2  |  DISEASES
6390  |  SDHB  |  DISEASES
6390  |  SDHB  |  DISEASES
727837  |  SSX2B  |  DISEASES
727837  |  SSX2B  |  DISEASES
6392  |  SDHD  |  DISEASES
6392  |  SDHD  |  DISEASES
728239  |  MAGED4  |  DISEASES
728239  |  MAGED4  |  DISEASES
3055  |  HCK  |  DISEASES
3055  |  HCK  |  DISEASES
343069  |  HNRNPCL1  |  DISEASES
343069  |  HNRNPCL1  |  DISEASES
50943  |  FOXP3  |  DISEASES
50943  |  FOXP3  |  DISEASES
100507436  |  MICA  |  DISEASES
100507436  |  MICA  |  DISEASES
56850  |  GRIPAP1  |  DISEASES
56850  |  GRIPAP1  |  DISEASES
648  |  BMI1  |  DISEASES
648  |  BMI1  |  DISEASES
4943  |  TBC1D25  |  DISEASES
4943  |  TBC1D25  |  DISEASES
3105  |  HLA-A  |  DISEASES
3105  |  HLA-A  |  DISEASES
11138  |  TBC1D8  |  DISEASES
11138  |  TBC1D8  |  DISEASES
1676  |  DFFA  |  DISEASES
1676  |  DFFA  |  DISEASES
80036  |  TRPM3  |  DISEASES
80036  |  TRPM3  |  DISEASES
6518  |  SLC2A5  |  DISEASES
6518  |  SLC2A5  |  DISEASES
3604  |  TNFRSF9  |  DISEASES
8241  |  RBM10  |  DISEASES
8241  |  RBM10  |  DISEASES
83715  |  ESPN  |  DISEASES
83715  |  ESPN  |  DISEASES
5100  |  PCDH8  |  DISEASES
5100  |  PCDH8  |  DISEASES
10590  |  SCGN  |  DISEASES
10590  |  SCGN  |  DISEASES
7403  |  KDM6A  |  DISEASES
7403  |  KDM6A  |  DISEASES
4609  |  MYC  |  DISEASES
4609  |  MYC  |  DISEASES
494188  |  FBXO47  |  DISEASES
494188  |  FBXO47  |  DISEASES
768  |  CA9  |  DISEASES
768  |  CA9  |  DISEASES
7102  |  TSPAN7  |  DISEASES
9308  |  CD83  |  DISEASES
9308  |  CD83  |  DISEASES
201725  |  C4orf46  |  DISEASES
201725  |  C4orf46  |  DISEASES
54438  |  GFOD1  |  DISEASES
54438  |  GFOD1  |  DISEASES
2625  |  GATA3  |  DISEASES
2625  |  GATA3  |  DISEASES
168400  |  DDX53  |  DISEASES
168400  |  DDX53  |  DISEASES
1906  |  EDN1  |  DISEASES
1906  |  EDN1  |  DISEASES
4739  |  NEDD9  |  DISEASES
4739  |  NEDD9  |  DISEASES
1543  |  CYP1A1  |  DISEASES
1543  |  CYP1A1  |  DISEASES
2683  |  B4GALT1  |  DISEASES
2683  |  B4GALT1  |  DISEASES
81567  |  TXNDC5  |  DISEASES
81567  |  TXNDC5  |  DISEASES
3559  |  IL2RA  |  DISEASES
3559  |  IL2RA  |  DISEASES
7010  |  TEK  |  DISEASES
7010  |  TEK  |  DISEASES
3445  |  IFNA8  |  DISEASES
3440  |  IFNA2  |  DISEASES
3440  |  IFNA2  |  DISEASES
3443  |  IFNA6  |  DISEASES
3446  |  IFNA10  |  DISEASES
3446  |  IFNA10  |  DISEASES
3452  |  IFNA21  |  DISEASES
3452  |  IFNA21  |  DISEASES
3467  |  IFNW1  |  DISEASES
3467  |  IFNW1  |  DISEASES
3456  |  IFNB1  |  DISEASES
3456  |  IFNB1  |  DISEASES
670  |  BPHL  |  DISEASES
670  |  BPHL  |  DISEASES
6194  |  RPS6  |  DISEASES
6194  |  RPS6  |  DISEASES
7114  |  TMSB4X  |  DISEASES
7114  |  TMSB4X  |  DISEASES
1045  |  CDX2  |  DISEASES
3486  |  IGFBP3  |  DISEASES
3486  |  IGFBP3  |  DISEASES
641372  |  ACOT6  |  DISEASES
641372  |  ACOT6  |  DISEASES
3709  |  ITPR2  |  DISEASES
3709  |  ITPR2  |  DISEASES
2315  |  MLANA  |  DISEASES
2315  |  MLANA  |  DISEASES
283820  |  NOMO2  |  DISEASES
283820  |  NOMO2  |  DISEASES
29126  |  CD274  |  DISEASES
29126  |  CD274  |  DISEASES
3717  |  JAK2  |  DISEASES
3717  |  JAK2  |  DISEASES
2576  |  GAGE4  |  DISEASES
2576  |  GAGE4  |  DISEASES
2543  |  GAGE1  |  DISEASES
2543  |  GAGE1  |  DISEASES
2280  |  FKBP1A  |  DISEASES
10457  |  GPNMB  |  DISEASES
10457  |  GPNMB  |  DISEASES
23600  |  AMACR  |  DISEASES
23600  |  AMACR  |  DISEASES
23189  |  KANK1  |  DISEASES
23189  |  KANK1  |  DISEASES
6624  |  FSCN1  |  DISEASES
6624  |  FSCN1  |  DISEASES
10232  |  MSLN  |  DISEASES
10232  |  MSLN  |  DISEASES
28512  |  NKIRAS1  |  DISEASES
28512  |  NKIRAS1  |  DISEASES
3875  |  KRT18  |  DISEASES
3875  |  KRT18  |  DISEASES
238  |  ALK  |  DISEASES
238  |  ALK  |  DISEASES
4017  |  LOXL2  |  DISEASES
4017  |  LOXL2  |  DISEASES
643236  |  TMEM72  |  DISEASES
643236  |  TMEM72  |  DISEASES
11100  |  HNRNPUL1  |  DISEASES
11100  |  HNRNPUL1  |  DISEASES
208  |  AKT2  |  DISEASES
9123  |  SLC16A3  |  DISEASES
9123  |  SLC16A3  |  DISEASES
326624  |  RAB37  |  DISEASES
326624  |  RAB37  |  DISEASES
7187  |  TRAF3  |  DISEASES
7187  |  TRAF3  |  DISEASES
80723  |  SLC35G2  |  DISEASES
80723  |  SLC35G2  |  DISEASES
654364  |  NME1-NME2  |  DISEASES
654364  |  NME1-NME2  |  DISEASES
4831  |  NME2  |  DISEASES
4831  |  NME2  |  DISEASES
10018  |  BCL2L11  |  DISEASES
10018  |  BCL2L11  |  DISEASES
4926  |  NUMA1  |  DISEASES
4926  |  NUMA1  |  DISEASES
56901  |  NDUFA4L2  |  DISEASES
56901  |  NDUFA4L2  |  DISEASES
3885  |  KRT34  |  DISEASES
3885  |  KRT34  |  DISEASES
307  |  ANXA4  |  DISEASES
307  |  ANXA4  |  DISEASES
55193  |  PBRM1  |  DISEASES
55193  |  PBRM1  |  DISEASES
6696  |  SPP1  |  DISEASES
6696  |  SPP1  |  DISEASES
51343  |  FZR1  |  DISEASES
51343  |  FZR1  |  DISEASES
983  |  CDK1  |  DISEASES
983  |  CDK1  |  DISEASES
3965  |  LGALS9  |  DISEASES
3965  |  LGALS9  |  DISEASES
10517  |  FBXW10  |  DISEASES
10517  |  FBXW10  |  DISEASES
174  |  AFP  |  DISEASES
174  |  AFP  |  DISEASES
6387  |  CXCL12  |  DISEASES
6387  |  CXCL12  |  DISEASES
5744  |  PTHLH  |  DISEASES
5744  |  PTHLH  |  DISEASES
7584  |  ZNF35  |  DISEASES
7584  |  ZNF35  |  DISEASES
79838  |  TMC5  |  DISEASES
79838  |  TMC5  |  DISEASES
116135  |  LRRC3B  |  DISEASES
116372  |  LYPD1  |  DISEASES
116372  |  LYPD1  |  DISEASES
80380  |  PDCD1LG2  |  DISEASES
80380  |  PDCD1LG2  |  DISEASES
5119  |  CHMP1A  |  DISEASES
5609  |  MAP2K7  |  DISEASES
5609  |  MAP2K7  |  DISEASES
2047  |  EPHB1  |  DISEASES
2047  |  EPHB1  |  DISEASES
153218  |  SPINK13  |  DISEASES
153218  |  SPINK13  |  DISEASES
2950  |  GSTP1  |  DISEASES
2950  |  GSTP1  |  DISEASES
23532  |  PRAME  |  DISEASES
23532  |  PRAME  |  DISEASES
408050  |  NOMO3  |  DISEASES
408050  |  NOMO3  |  DISEASES
6093  |  ROCK1  |  DISEASES
6093  |  ROCK1  |  DISEASES
134111  |  UBE2QL1  |  DISEASES
134111  |  UBE2QL1  |  DISEASES
100287898  |  TTC34  |  DISEASES
100287898  |  TTC34  |  DISEASES
9612  |  NCOR2  |  DISEASES
9612  |  NCOR2  |  DISEASES
54891  |  INO80D  |  DISEASES
54891  |  INO80D  |  DISEASES
5970  |  RELA  |  DISEASES
5970  |  RELA  |  DISEASES
95  |  ACY1  |  DISEASES
95  |  ACY1  |  DISEASES
1994  |  ELAVL1  |  DISEASES
1994  |  ELAVL1  |  DISEASES
728441  |  GGT2  |  DISEASES
728441  |  GGT2  |  DISEASES
26173  |  INTS1  |  DISEASES
26173  |  INTS1  |  DISEASES
2011  |  MARK2  |  DISEASES
55627  |  SMPD4  |  DISEASES
55627  |  SMPD4  |  DISEASES
29072  |  SETD2  |  DISEASES
29072  |  SETD2  |  DISEASES
7852  |  CXCR4  |  DISEASES
7852  |  CXCR4  |  DISEASES
1385  |  CREB1  |  DISEASES
1385  |  CREB1  |  DISEASES
3384  |  ICAM2  |  DISEASES
3384  |  ICAM2  |  DISEASES
79744  |  ZNF419  |  DISEASES
79744  |  ZNF419  |  DISEASES
1630  |  DCC  |  DISEASES
1630  |  DCC  |  DISEASES
155006  |  TMEM213  |  DISEASES
155006  |  TMEM213  |  DISEASES
4495  |  MT1G  |  DISEASES
4495  |  MT1G  |  DISEASES
64098  |  PARVG  |  DISEASES
64098  |  PARVG  |  DISEASES
3718  |  JAK3  |  DISEASES
3718  |  JAK3  |  DISEASES
3481  |  IGF2  |  DISEASES
3481  |  IGF2  |  DISEASES
100144748  |  KLLN  |  DISEASES
100144748  |  KLLN  |  DISEASES
2260  |  FGFR1  |  DISEASES
2260  |  FGFR1  |  DISEASES
4988  |  OPRM1  |  DISEASES
4988  |  OPRM1  |  DISEASES
1029  |  CDKN2A  |  DISEASES
1029  |  CDKN2A  |  DISEASES
7849  |  PAX8  |  DISEASES
7849  |  PAX8  |  DISEASES
25959  |  KANK2  |  DISEASES
25959  |  KANK2  |  DISEASES
387836  |  CLEC2A  |  DISEASES
387836  |  CLEC2A  |  DISEASES
5076  |  PAX2  |  DISEASES
5076  |  PAX2  |  DISEASES
10725  |  NFAT5  |  DISEASES
10725  |  NFAT5  |  DISEASES
4696  |  NDUFA3  |  DISEASES
4696  |  NDUFA3  |  DISEASES
56616  |  DIABLO  |  DISEASES
960  |  CD44  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
7124  |  TNF  |  DISEASES
6304  |  SATB1  |  DISEASES
6304  |  SATB1  |  DISEASES
2130  |  EWSR1  |  DISEASES
387  |  RHOA  |  DISEASES
387  |  RHOA  |  DISEASES
6490  |  PMEL  |  DISEASES
6490  |  PMEL  |  DISEASES
29970  |  SCHIP1  |  DISEASES
29970  |  SCHIP1  |  DISEASES
91833  |  WDR20  |  DISEASES
91833  |  WDR20  |  DISEASES
7266  |  DNAJC7  |  DISEASES
7266  |  DNAJC7  |  DISEASES
57862  |  ZNF410  |  DISEASES
57862  |  ZNF410  |  DISEASES
10969  |  EBNA1BP2  |  DISEASES
10969  |  EBNA1BP2  |  DISEASES
154664  |  ABCA13  |  DISEASES
154664  |  ABCA13  |  DISEASES
3451  |  IFNA17  |  DISEASES
3451  |  IFNA17  |  DISEASES
3586  |  IL10  |  DISEASES
3586  |  IL10  |  DISEASES
80319  |  CXXC4  |  DISEASES
80319  |  CXXC4  |  DISEASES
58155  |  PTBP2  |  DISEASES
8842  |  PROM1  |  DISEASES
8842  |  PROM1  |  DISEASES
6513  |  SLC2A1  |  DISEASES
6513  |  SLC2A1  |  DISEASES
7045  |  TGFBI  |  DISEASES
7045  |  TGFBI  |  DISEASES
4753  |  NELL2  |  DISEASES
4753  |  NELL2  |  DISEASES
8314  |  BAP1  |  DISEASES
8314  |  BAP1  |  DISEASES
4193  |  MDM2  |  DISEASES
4193  |  MDM2  |  DISEASES
11279  |  KLF8  |  DISEASES
11279  |  KLF8  |  DISEASES
5793  |  PTPRG  |  DISEASES
5793  |  PTPRG  |  DISEASES
6256  |  RXRA  |  DISEASES
6256  |  RXRA  |  DISEASES
127933  |  UHMK1  |  DISEASES
96459  |  FNIP1  |  DISEASES
96459  |  FNIP1  |  DISEASES
9353  |  SLIT2  |  DISEASES
9353  |  SLIT2  |  DISEASES
1977  |  EIF4E  |  DISEASES
1977  |  EIF4E  |  DISEASES
284  |  ANGPT1  |  DISEASES
284  |  ANGPT1  |  DISEASES
138046  |  RALYL  |  DISEASES
138046  |  RALYL  |  DISEASES
6586  |  SLIT3  |  DISEASES
6586  |  SLIT3  |  DISEASES
533  |  ATP6V0B  |  DISEASES
533  |  ATP6V0B  |  DISEASES
55845  |  BRK1  |  DISEASES
55845  |  BRK1  |  DISEASES
28970  |  C11orf54  |  DISEASES
28970  |  C11orf54  |  DISEASES
8693  |  GALNT4  |  DISEASES
8693  |  GALNT4  |  DISEASES
930  |  CD19  |  DISEASES
930  |  CD19  |  DISEASES
283212  |  KLHL35  |  DISEASES
283212  |  KLHL35  |  DISEASES
7694  |  ZNF135  |  DISEASES
7694  |  ZNF135  |  DISEASES
3684  |  ITGAM  |  DISEASES
3684  |  ITGAM  |  DISEASES
8284  |  KDM5D  |  DISEASES
8284  |  KDM5D  |  DISEASES
8453  |  CUL2  |  DISEASES
8453  |  CUL2  |  DISEASES
3939  |  LDHA  |  DISEASES
3939  |  LDHA  |  DISEASES
201266  |  SLC39A11  |  DISEASES
201266  |  SLC39A11  |  DISEASES
3227  |  HOXC11  |  DISEASES
7421  |  VDR  |  DISEASES
7421  |  VDR  |  DISEASES
89894  |  TMEM116  |  DISEASES
89894  |  TMEM116  |  DISEASES
317  |  APAF1  |  DISEASES
317  |  APAF1  |  DISEASES
5228  |  PGF  |  DISEASES
5228  |  PGF  |  DISEASES
567  |  B2M  |  DISEASES
567  |  B2M  |  DISEASES
7732  |  RNF112  |  DISEASES
7732  |  RNF112  |  DISEASES
388630  |  TRABD2B  |  DISEASES
388630  |  TRABD2B  |  DISEASES
51741  |  WWOX  |  DISEASES
51741  |  WWOX  |  DISEASES
3316  |  HSPB2  |  DISEASES
3316  |  HSPB2  |  DISEASES
391104  |  VHLL  |  DISEASES
391104  |  VHLL  |  DISEASES
126520  |  PLK5  |  DISEASES
126520  |  PLK5  |  DISEASES
10975  |  UQCR11  |  DISEASES
10975  |  UQCR11  |  DISEASES
65982  |  ZSCAN18  |  DISEASES
65982  |  ZSCAN18  |  DISEASES
100750247  |  HIF1A-AS2  |  DISEASES
100124700  |  HOTAIR  |  DISEASES
401253  |  LINC00336  |  DISEASES
401253  |  LINC00336  |  DISEASES
100302640  |  LINC00882  |  DISEASES
100302640  |  LINC00882  |  DISEASES
100506190  |  LINC00963  |  DISEASES
100506190  |  LINC00963  |  DISEASES
440556  |  LINC00982  |  DISEASES
440556  |  LINC00982  |  DISEASES
378938  |  MALAT1  |  DISEASES
378938  |  MALAT1  |  DISEASES
729177  |  NBAT1  |  DISEASES
729177  |  NBAT1  |  DISEASES
283131  |  NEAT1  |  DISEASES
283131  |  NEAT1  |  DISEASES
101241892  |  NPTN-IT1  |  DISEASES
101154753  |  PANDAR  |  DISEASES
101154753  |  PANDAR  |  DISEASES
104472713  |  PCAT29  |  DISEASES
104472713  |  PCAT29  |  DISEASES
5820  |  PVT1  |  DISEASES
84973  |  SNHG7  |  DISEASES
84973  |  SNHG7  |  DISEASES
26821  |  SNORA74A  |  DISEASES
26821  |  SNORA74A  |  DISEASES
727676  |  SNORD118  |  DISEASES
677848  |  SNORD1A  |  DISEASES
677848  |  SNORD1A  |  DISEASES
26806  |  SNORD44  |  DISEASES
26806  |  SNORD44  |  DISEASES
26801  |  SNORD48  |  DISEASES
26801  |  SNORD48  |  DISEASES
619498  |  SNORD74  |  DISEASES
619498  |  SNORD74  |  DISEASES
27004  |  TCL6  |  DISEASES
27004  |  TCL6  |  DISEASES
200197  |  TMEM51-AS1  |  DISEASES
200197  |  TMEM51-AS1  |  DISEASES
100507602  |  TRIM52-AS1  |  DISEASES
100507602  |  TRIM52-AS1  |  DISEASES
55000  |  TUG1  |  DISEASES
55000  |  TUG1  |  DISEASES
Locus(Waiting for update.)
Disease ID 28
Disease renal cell carcinoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:102)
HP:0002664  |  Neoplasia  |  135
HP:0003774  |  End-stage renal failure  |  13
HP:0001513  |  Obesity  |  10
HP:0030731  |  Carcinoma  |  9
HP:0001907  |  Thromboembolic disease  |  7
HP:0012622  |  Chronic kidney disease  |  7
HP:0000822  |  Hypertension  |  6
HP:0002835  |  Aspiration  |  5
HP:0001082  |  Cholecystitis  |  4
HP:0012126  |  Gastric cancer  |  4
HP:0000821  |  Underactive thyroid  |  3
HP:0001541  |  Ascites  |  3
HP:0001635  |  Congestive heart failure  |  3
HP:0000819  |  Diabetes mellitus  |  3
HP:0001894  |  Thrombocytosis  |  3
HP:0009726  |  Renal neoplasm  |  3
HP:0012034  |  Liposarcoma  |  3
HP:0002669  |  Osteosarcoma  |  3
HP:0002861  |  Melanoma  |  2
HP:0001217  |  Digital clubbing  |  2
HP:0000979  |  Purpura  |  2
HP:0001903  |  Anemia  |  2
HP:0000718  |  Aggressive behaviour  |  2
HP:0000085  |  Horseshoe kidney  |  2
HP:0002665  |  Lymphoma  |  2
HP:0010797  |  Hemangioblastoma  |  2
HP:0002176  |  Spinal cord compression  |  2
HP:0000083  |  Renal insufficiency  |  2
HP:0000086  |  Ectopic kidney  |  2
HP:0012531  |  Pain  |  2
HP:0006772  |  Angiomyolipoma  |  2
HP:0005584  |  Renal cell carcinoma  |  2
HP:0012378  |  Fatigue  |  2
HP:0000113  |  Polycystic kidney dysplasia  |  2
HP:0006770  |  Nonpapillary renal cell carcinoma  |  2
HP:0002015  |  Swallowing difficulty  |  1
HP:0002204  |  Pulmonary embolism  |  1
HP:0100658  |  Bacterial infection of skin  |  1
HP:0100633  |  Inflammation of the esophagus  |  1
HP:0001945  |  Fever  |  1
HP:0012189  |  Hodgkin disease  |  1
HP:0003201  |  Rhabdomyolysis  |  1
HP:0100727  |  Histiocytosis  |  1
HP:0002647  |  Aortic dissection  |  1
HP:0002090  |  Pneumonia  |  1
HP:0040184  |  Oral hemorrhage  |  1
HP:0002890  |  Thyroid carcinoma  |  1
HP:0002105  |  Hemoptysis  |  1
HP:0012636  |  Retinal vein occlusion  |  1
HP:0001028  |  Strawberry mark  |  1
HP:0001402  |  Hepatocellular carcinoma  |  1
HP:0100759  |  Finger clubbing  |  1
HP:0002896  |  Liver cancer  |  1
HP:0002667  |  Wilms tumor  |  1
HP:0011798  |  Renal oncocytoma  |  1
HP:0005145  |  Narrowing of coronary artery  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0010566  |  Hamartoma  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0000100  |  Nephrosis  |  1
HP:0012156  |  Hemophagocytosis  |  1
HP:0006766  |  Papillary renal cell carcinoma  |  1
HP:0001901  |  Abnormally shaped erythrocytes  |  1
HP:0000952  |  Yellow skin  |  1
HP:0002584  |  Intestinal hemorrhage  |  1
HP:0001369  |  Arthritis  |  1
HP:0002239  |  Gastrointestinal hemorrhage  |  1
HP:0001396  |  Cholestasis  |  1
HP:0001978  |  Extramedullary hematopoiesis  |  1
HP:0011974  |  Myelofibrosis  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0002249  |  Melena  |  1
HP:0003073  |  Hypoalbuminaemia  |  1
HP:0003072  |  Hypercalcemia  |  1
HP:0009733  |  Glioma  |  1
HP:0100697  |  Neurofibrosarcoma  |  1
HP:0001880  |  Eosinophilia  |  1
HP:0030839  |  Knee pain  |  1
HP:0009725  |  Bladder neoplasm  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0002901  |  Hypocalcemia  |  1
HP:0001004  |  Lymphatic obstruction  |  1
HP:0011349  |  Sixth nerve palsy  |  1
HP:0001882  |  Decreased blood leukocyte number  |  1
HP:0000107  |  Renal cyst  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0003473  |  Fatigable weakness  |  1
HP:0005306  |  Capillary hemangioma  |  1
HP:0002902  |  Hyponatremia  |  1
HP:0001873  |  Low platelet count  |  1
HP:0002027  |  Abdominal pain  |  1
HP:0001289  |  Confusion  |  1
HP:0200023  |  Priapism  |  1
HP:0005200  |  Retroperitoneal fibrosis  |  1
HP:0001919  |  Acute renal failure  |  1
HP:0000738  |  Sensory hallucination  |  1
HP:0001138  |  Damaged optic nerve  |  1
HP:0000421  |  Bloody nose  |  1
HP:0002633  |  Vasculitis  |  1
HP:0030242  |  Blood clot in portal vein  |  1
HP:0012539  |  Non-Hodgkin lymphoma  |  1
HP:0002576  |  Intussusception  |  1
Disease ID 28
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:51)
C0040053  |  thrombus  |  46
C0153690  |  bone metastasis  |  12
C0028754  |  obesity  |  10
C0153690  |  bone metastases  |  8
C0153676  |  lung metastases  |  7
C0019562  |  von hippel-lindau disease  |  7
C0153676  |  pulmonary metastasis  |  6
C0002793  |  dedifferentiation  |  6
C0153676  |  lung metastasis  |  6
C0220650  |  brain metastases  |  5
C1332335  |  arterial embolization  |  4
C0220650  |  brain metastasis  |  4
C0018801  |  heart failure  |  3
C0019562  |  von hippel lindau disease  |  3
C0022665  |  renal tumors  |  3
C0153676  |  pulmonary metastases  |  3
C0153687  |  cutaneous metastasis  |  3
C0836924  |  thrombocytosis  |  3
C0153685  |  renal metastasis  |  3
C2119038  |  pleural metastasis  |  2
C0494165  |  liver metastases  |  2
C0016169  |  fistula  |  2
C0686619  |  lymph node metastases  |  2
C0155776  |  renal vein thrombosis  |  2
C0030193  |  pain  |  2
C0854178  |  adrenal metastases  |  2
C0030472  |  paraneoplastic syndrome  |  2
C0018952  |  extramedullary hematopoiesis  |  1
C0741299  |  atrial thrombus  |  1
C0023903  |  liver tumor  |  1
C0085652  |  pyoderma gangrenosum  |  1
C0022679  |  renal cyst  |  1
C0019080  |  hemorrhage  |  1
C0032227  |  pleural effusion  |  1
C0020437  |  hypercalcemia  |  1
C0034065  |  pulmonary embolism  |  1
C0003873  |  rheumatoid arthritis  |  1
C0027149  |  myxoma  |  1
C0521607  |  peritoneal fibrosis  |  1
C0268799  |  acquired renal cystic disease  |  1
C0346255  |  renal oncocytoma  |  1
C0346976  |  pancreatic metastasis  |  1
C0333516  |  tumor necrosis  |  1
C1335745  |  renal liposarcoma  |  1
C1609519  |  adrenal myelolipoma  |  1
C0153687  |  skin metastasis  |  1
C0494165  |  liver metastasis  |  1
C0002871  |  anemia  |  1
C0015967  |  fever  |  1
C0267373  |  intestinal bleeding  |  1
C0206635  |  myelolipoma  |  1
Manually Genotype(Total Text Mining 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:1)
HP ID HP Name MP ID MP Name Annotation
HP:0001978Extramedullary hematopoiesisMP:0000240extramedullary hematopoiesis;HP:0001919Acute kidney injury
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0002716LymphadenopathyMP:0002420abnormal adaptive immunity;HP:0001894Thrombocytosis
Chemical(Total Drugs:24)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0007134acetaminophenD000082103-90-2carcinoma, renal cellMESH:D002292marker/mechanism10507783
C0007134celecoxibD000068579-carcinoma, renal cellMESH:D002292therapeutic16369983
C0007134cyclophosphamideD00352050-18-0carcinoma, renal cellMESH:D002292marker/mechanism8996475
C0007134cyclophosphamideD00352050-18-0carcinoma, renal cellMESH:D002292therapeutic16201981
C0007134diethylstilbestrolD00405456-53-1carcinoma, renal cellMESH:D002292marker/mechanism2650911
C0007134everolimusD000068338-carcinoma, renal cellMESH:D002292therapeutic18653228
C0007134fluorouracilD00547251-21-8carcinoma, renal cellMESH:D002292therapeutic15895229
C0007134folic acidD00549259-30-3carcinoma, renal cellMESH:D002292therapeutic10663624
C0007134gemcitabineC056507103882-84-4carcinoma, renal cellMESH:D002292therapeutic15895229
C0007134hydroxyureaD006918127-07-1carcinoma, renal cellMESH:D002292therapeutic4883783
C0007134ifosfamideD0070693778-73-2carcinoma, renal cellMESH:D002292therapeutic6495457
C0007134indomethacinD00721353-86-1carcinoma, renal cellMESH:D002292therapeutic17341418
C0007134medroxyprogesterone acetateD01725871-58-9carcinoma, renal cellMESH:D002292therapeutic1152883
C0007134pazopanibC516667-carcinoma, renal cellMESH:D002292therapeutic19956806
C0007134peginterferon alfa-2bC417083-carcinoma, renal cellMESH:D002292therapeutic18813777
C0007134sorafenibC471405-carcinoma, renal cellMESH:D002292therapeutic18695262
C0007134streptozocinD01331118883-66-4carcinoma, renal cellMESH:D002292marker/mechanism128413
C0007134temsirolimusC401859-carcinoma, renal cellMESH:D002292therapeutic19232474
C0007134thalidomideD01379250-35-1carcinoma, renal cellMESH:D002292therapeutic11592764
C0007134toremifeneD01731289778-26-7carcinoma, renal cellMESH:D002292marker/mechanism7586193
C0007134vinblastineD014747865-21-4carcinoma, renal cellMESH:D002292therapeutic1485588
C0007134vincristineD014750-carcinoma, renal cellMESH:D002292therapeutic16201981
C0007134vindesineD01475153643-48-4carcinoma, renal cellMESH:D002292therapeutic2930717
C0007134zoledronic acidC088658-carcinoma, renal cellMESH:D002292therapeutic17070308
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)