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PedAM

Pediatric Disease Annotations & Medicines



   wilms tumor
  

Disease ID 169
Disease wilms tumor
Definition
pediatric nephroblastoma originating from embryonic kidney stem cells; usually affects children before the fifth year, but may occur in the fetus or rarely in later life; caused by defects in one or more tumor suppressor genes.
Synonym
[m]nephroblastoma nos
embryonal adenosarcoma
embryonal nephroma
kidney wilms tumor
kidney, adenomyosarcoma, embryonal
kidney, carcinosarcoma, embryonal
kidney, embryoma
kidney, embryonal mixed tumor
nephroblastoma
nephroblastoma (disorder)
nephroblastoma (m-89603)
nephroblastoma (morphologic abnormality)
nephroblastoma (wilms tumor)
nephroblastoma, malignant
nephroblastoma, nos
nephroblastomas
nephroma
nephroma, nos
nephromas
perlman syndrome
renal adenosarcoma
renal cancer, wilms
renal wilms tumor
renal wilms' tumor
tumor wilm's
tumor wilms
tumor wilms'
tumor wilms's
tumor, wilms
tumor, wilms'
tumors wilm's
tumors wilms
wilm tumor
wilm's tumor
wilms tumor (nephroblastoma)
wilms tumor 1
wilms tumor [disease/finding]
wilms tumor of the kidney
wilms tumour
wilms' tumor
wilms' tumor and other childhood kidney tumors
wilms' tumor of the kidney
wilms' tumour
wt1
Orphanet
OMIM
DOID
UMLS
C0027708
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:34)
C0040053  |  thrombus  |  2
C0153676  |  lung metastasis  |  2
C0022972  |  lambert-eaton myasthenic syndrome  |  1
C0950121  |  denys-drash syndrome  |  1
C0555198  |  malignant gliomas  |  1
C0153676  |  pulmonary metastases  |  1
C0677886  |  epithelial ovarian cancer  |  1
C0039446  |  telangiectasia  |  1
C0152096  |  trisomy 18  |  1
C0022658  |  renal disease  |  1
C0153676  |  lung metastases  |  1
C0027819  |  neuroblastoma  |  1
C1370740  |  adrenal carcinoma  |  1
C0006142  |  breast cancer  |  1
C0007134  |  renal carcinoma  |  1
C1140680  |  ovarian ca  |  1
C0023418  |  leukemia  |  1
C0020598  |  hypoglycaemia  |  1
C0392784  |  dermatofibrosarcoma protuberans  |  1
C0041341  |  tuberous sclerosis complex  |  1
C1140680  |  ovarian cancer  |  1
C0950121  |  drash syndrome  |  1
C0004134  |  ataxia  |  1
C0555198  |  malignant glioma  |  1
C0740394  |  hyperuricemia  |  1
C0024115  |  lung disease  |  1
C0022972  |  myasthenic syndrome  |  1
C0004779  |  gorlin syndrome  |  1
C0041341  |  tuberous sclerosis  |  1
C0022661  |  end stage renal disease  |  1
C0015625  |  fanconi anemia  |  1
C0002871  |  anemia  |  1
C0010481  |  cushing syndrome  |  1
C0008479  |  chondrosarcoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:16)
BRCA2  |  675  |  CTD_human
IGF2  |  3481  |  CTD_human
WT1  |  7490  |  CTD_human;OMIM;ORPHANET;UNIPROT
NHS  |  4810  |  GWASCAT
TCN2  |  6948  |  GWASCAT
PCSK9  |  255738  |  GWASCAT
GPC3  |  2719  |  CTD_human
CTNNB1  |  1499  |  CTD_human
DDX1  |  1653  |  GWASCAT
GLIPR1  |  11010  |  CTD_human
VHL  |  7428  |  CTD_human
H19  |  283120  |  ORPHANET
POU6F2  |  11281  |  ORPHANET
DIS3L2  |  129563  |  ORPHANET
REST  |  5978  |  CTD_human;ORPHANET
DLG2  |  1740  |  GWASCAT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
7490  |  WT1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:409)
618  |  BCYRN1  |  DISEASES
928  |  CD9  |  DISEASES
4826  |  NNAT  |  DISEASES
54432  |  YIPF1  |  DISEASES
3784  |  KCNQ1  |  DISEASES
9319  |  TRIP13  |  DISEASES
54474  |  KRT20  |  DISEASES
2099  |  ESR1  |  DISEASES
25776  |  CBY1  |  DISEASES
10914  |  PAPOLA  |  DISEASES
57167  |  SALL4  |  DISEASES
6725  |  SRMS  |  DISEASES
58189  |  WFDC1  |  DISEASES
56915  |  EXOSC5  |  DISEASES
268  |  AMH  |  DISEASES
7040  |  TGFB1  |  DISEASES
1048  |  CEACAM5  |  DISEASES
199731  |  CADM4  |  DISEASES
2645  |  GCK  |  DISEASES
733  |  C8G  |  DISEASES
1440  |  CSF3  |  DISEASES
10014  |  HDAC5  |  DISEASES
8929  |  PHOX2B  |  DISEASES
3558  |  IL2  |  DISEASES
1410  |  CRYAB  |  DISEASES
595  |  CCND1  |  DISEASES
1027  |  CDKN1B  |  DISEASES
3458  |  IFNG  |  DISEASES
2597  |  GAPDH  |  DISEASES
2026  |  ENO2  |  DISEASES
26271  |  FBXO5  |  DISEASES
1653  |  DDX1  |  DISEASES
5657  |  PRTN3  |  DISEASES
7799  |  PRDM2  |  DISEASES
6943  |  TCF21  |  DISEASES
5918  |  RARRES1  |  DISEASES
9525  |  VPS4B  |  DISEASES
84272  |  YIPF4  |  DISEASES
1958  |  EGR1  |  DISEASES
847  |  CAT  |  DISEASES
2322  |  FLT3  |  DISEASES
4656  |  MYOG  |  DISEASES
1959  |  EGR2  |  DISEASES
1026  |  CDKN1A  |  DISEASES
6662  |  SOX9  |  DISEASES
7389  |  UROD  |  DISEASES
6495  |  SIX1  |  DISEASES
3976  |  LIF  |  DISEASES
8854  |  ALDH1A2  |  DISEASES
4654  |  MYOD1  |  DISEASES
6299  |  SALL1  |  DISEASES
56097  |  PCDHGC5  |  DISEASES
3852  |  KRT5  |  DISEASES
81  |  ACTN4  |  DISEASES
9253  |  NUMBL  |  DISEASES
78992  |  YIPF2  |  DISEASES
10343  |  PKDREJ  |  DISEASES
10343  |  PKDREJ  |  DISEASES
5914  |  RARA  |  DISEASES
2488  |  FSHB  |  DISEASES
79727  |  LIN28A  |  DISEASES
79727  |  LIN28A  |  DISEASES
3975  |  LHX1  |  DISEASES
8900  |  CCNA1  |  DISEASES
5920  |  RARRES3  |  DISEASES
10752  |  CHL1  |  DISEASES
23318  |  ZCCHC11  |  DISEASES
5156  |  PDGFRA  |  DISEASES
9883  |  POM121  |  DISEASES
79056  |  PRRG4  |  DISEASES
3569  |  IL6  |  DISEASES
28969  |  BZW2  |  DISEASES
4856  |  NOV  |  DISEASES
5460  |  POU5F1  |  DISEASES
23213  |  SULF1  |  DISEASES
7057  |  THBS1  |  DISEASES
1588  |  CYP19A1  |  DISEASES
9585  |  KIF20B  |  DISEASES
894  |  CCND2  |  DISEASES
79728  |  PALB2  |  DISEASES
1800  |  DPEP1  |  DISEASES
999  |  CDH1  |  DISEASES
945  |  CD33  |  DISEASES
29855  |  UBN1  |  DISEASES
26001  |  RNF167  |  DISEASES
23361  |  ZNF629  |  DISEASES
57531  |  HACE1  |  DISEASES
1871  |  E2F3  |  DISEASES
6598  |  SMARCB1  |  DISEASES
8424  |  BBOX1  |  DISEASES
54487  |  DGCR8  |  DISEASES
6855  |  SYP  |  DISEASES
975  |  CD81  |  DISEASES
4072  |  EPCAM  |  DISEASES
55850  |  USE1  |  DISEASES
10664  |  CTCF  |  DISEASES
2817  |  GPC1  |  DISEASES
60482  |  SLC5A7  |  DISEASES
374  |  AREG  |  DISEASES
6774  |  STAT3  |  DISEASES
10923  |  SUB1  |  DISEASES
51176  |  LEF1  |  DISEASES
7472  |  WNT2  |  DISEASES
5395  |  PMS2  |  DISEASES
11010  |  GLIPR1  |  DISEASES
22822  |  PHLDA1  |  DISEASES
3480  |  IGF1R  |  DISEASES
7727  |  ZNF174  |  DISEASES
7157  |  TP53  |  DISEASES
2064  |  ERBB2  |  DISEASES
207  |  AKT1  |  DISEASES
126374  |  WTIP  |  DISEASES
83540  |  NUF2  |  DISEASES
5546  |  PRCC  |  DISEASES
5972  |  REN  |  DISEASES
890  |  CCNA2  |  DISEASES
1956  |  EGFR  |  DISEASES
4915  |  NTRK2  |  DISEASES
2620  |  GAS2  |  DISEASES
22948  |  CCT5  |  DISEASES
4613  |  MYCN  |  DISEASES
5800  |  PTPRO  |  DISEASES
5458  |  POU4F2  |  DISEASES
55294  |  FBXW7  |  DISEASES
23091  |  ZC3H13  |  DISEASES
7070  |  THY1  |  DISEASES
7071  |  KLF10  |  DISEASES
8324  |  FZD7  |  DISEASES
9246  |  UBE2L6  |  DISEASES
701  |  BUB1B  |  DISEASES
8321  |  FZD1  |  DISEASES
3815  |  KIT  |  DISEASES
54361  |  WNT4  |  DISEASES
3856  |  KRT8  |  DISEASES
213  |  ALB  |  DISEASES
25976  |  TIPARP  |  DISEASES
134288  |  TMEM174  |  DISEASES
4869  |  NPM1  |  DISEASES
168667  |  BMPER  |  DISEASES
116039  |  OSR2  |  DISEASES
11244  |  ZHX1  |  DISEASES
56339  |  METTL3  |  DISEASES
26610  |  ELP4  |  DISEASES
9317  |  PTER  |  DISEASES
54765  |  TRIM44  |  DISEASES
861  |  RUNX1  |  DISEASES
6786  |  STIM1  |  DISEASES
353514  |  LILRA5  |  DISEASES
3960  |  LGALS4  |  DISEASES
3233  |  HOXD4  |  DISEASES
598  |  BCL2L1  |  DISEASES
8796  |  SCEL  |  DISEASES
3479  |  IGF1  |  DISEASES
7324  |  UBE2E1  |  DISEASES
90075  |  ZNF30  |  DISEASES
10736  |  SIX2  |  DISEASES
1495  |  CTNNA1  |  DISEASES
25928  |  SOSTDC1  |  DISEASES
2353  |  FOS  |  DISEASES
794  |  CALB2  |  DISEASES
51068  |  NMD3  |  DISEASES
5002  |  SLC22A18  |  DISEASES
11338  |  U2AF2  |  DISEASES
27087  |  B3GAT1  |  DISEASES
64852  |  TUT1  |  DISEASES
7015  |  TERT  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
9610  |  RIN1  |  DISEASES
5098  |  PCDHGC3  |  DISEASES
79870  |  BAALC  |  DISEASES
3172  |  HNF4A  |  DISEASES
80818  |  ZNF436  |  DISEASES
7030  |  TFE3  |  DISEASES
129563  |  DIS3L2  |  DISEASES
129563  |  DIS3L2  |  DISEASES
23541  |  SEC14L2  |  DISEASES
4302  |  MLLT6  |  DISEASES
50649  |  ARHGEF4  |  DISEASES
4233  |  MET  |  DISEASES
9702  |  CEP57  |  DISEASES
1960  |  EGR3  |  DISEASES
4684  |  NCAM1  |  DISEASES
7262  |  PHLDA2  |  DISEASES
10409  |  BASP1  |  DISEASES
2146  |  EZH2  |  DISEASES
10782  |  ZNF274  |  DISEASES
4222  |  MEOX1  |  DISEASES
115752  |  DIS3L  |  DISEASES
115752  |  DIS3L  |  DISEASES
10611  |  PDLIM5  |  DISEASES
387758  |  FIBIN  |  DISEASES
8938  |  BAIAP3  |  DISEASES
148266  |  ZNF569  |  DISEASES
5241  |  PGR  |  DISEASES
7481  |  WNT11  |  DISEASES
58531  |  PRM3  |  DISEASES
2863  |  GPR39  |  DISEASES
5074  |  PAWR  |  DISEASES
3855  |  KRT7  |  DISEASES
83999  |  KREMEN1  |  DISEASES
7490  |  WT1  |  DISEASES
7490  |  WT1  |  DISEASES
942  |  CD86  |  DISEASES
430  |  ASCL2  |  DISEASES
5727  |  PTCH1  |  DISEASES
60529  |  ALX4  |  DISEASES
3916  |  LAMP1  |  DISEASES
266740  |  MAGEA2B  |  DISEASES
6297  |  SALL2  |  DISEASES
148103  |  ZNF599  |  DISEASES
3043  |  HBB  |  DISEASES
2626  |  GATA4  |  DISEASES
338645  |  LUZP2  |  DISEASES
4664  |  NAB1  |  DISEASES
6940  |  ZNF354A  |  DISEASES
7767  |  ZNF224  |  DISEASES
7016  |  TESK1  |  DISEASES
29102  |  DROSHA  |  DISEASES
4602  |  MYB  |  DISEASES
966  |  CD59  |  DISEASES
57175  |  CORO1B  |  DISEASES
8788  |  DLK1  |  DISEASES
3167  |  HMX2  |  DISEASES
5764  |  PTN  |  DISEASES
2138  |  EYA1  |  DISEASES
23405  |  DICER1  |  DISEASES
23405  |  DICER1  |  DISEASES
389421  |  LIN28B  |  DISEASES
1499  |  CTNNB1  |  DISEASES
9158  |  FIBP  |  DISEASES
3767  |  KCNJ11  |  DISEASES
797  |  CALCB  |  DISEASES
2109  |  ETFB  |  DISEASES
6275  |  S100A4  |  DISEASES
5154  |  PDGFA  |  DISEASES
9967  |  THRAP3  |  DISEASES
7080  |  NKX2-1  |  DISEASES
6666  |  SOX12  |  DISEASES
4010  |  LMX1B  |  DISEASES
51710  |  ZNF44  |  DISEASES
8736  |  MYOM1  |  DISEASES
11186  |  RASSF1  |  DISEASES
60  |  ACTB  |  DISEASES
9961  |  MVP  |  DISEASES
744  |  MPPED2  |  DISEASES
23567  |  ZNF346  |  DISEASES
4763  |  NF1  |  DISEASES
9589  |  WTAP  |  DISEASES
2526  |  FUT4  |  DISEASES
55243  |  KIRREL  |  DISEASES
23607  |  CD2AP  |  DISEASES
4151  |  MB  |  DISEASES
4192  |  MDK  |  DISEASES
4311  |  MME  |  DISEASES
6533  |  SLC6A6  |  DISEASES
51222  |  ZNF219  |  DISEASES
4916  |  NTRK3  |  DISEASES
10256  |  CNKSR1  |  DISEASES
6665  |  SOX15  |  DISEASES
57829  |  ZP4  |  DISEASES
7107  |  GPR137B  |  DISEASES
148811  |  PM20D1  |  DISEASES
89796  |  NAV1  |  DISEASES
2494  |  NR5A2  |  DISEASES
5788  |  PTPRC  |  DISEASES
56956  |  LHX9  |  DISEASES
79577  |  CDC73  |  DISEASES
10625  |  IVNS1ABP  |  DISEASES
54823  |  SWT1  |  DISEASES
777  |  CACNA1E  |  DISEASES
7827  |  NPHS2  |  DISEASES
1490  |  CTGF  |  DISEASES
93183  |  PIGM  |  DISEASES
1382  |  CRABP2  |  DISEASES
10763  |  NES  |  DISEASES
10654  |  PMVK  |  DISEASES
256536  |  TCERG1L  |  DISEASES
126961  |  HIST2H3C  |  DISEASES
3283  |  HSD3B1  |  DISEASES
474384  |  F8A3  |  DISEASES
474383  |  F8A2  |  DISEASES
4803  |  NGF  |  DISEASES
4893  |  NRAS  |  DISEASES
64858  |  DCLRE1B  |  DISEASES
10745  |  PHTF1  |  DISEASES
9096  |  TBX18  |  DISEASES
9748  |  SLK  |  DISEASES
4102  |  MAGEA3  |  DISEASES
4101  |  MAGEA2  |  DISEASES
2239  |  GPC4  |  DISEASES
2239  |  GPC4  |  DISEASES
84612  |  PARD6B  |  DISEASES
7422  |  VEGFA  |  DISEASES
25  |  ABL1  |  DISEASES
25844  |  YIPF3  |  DISEASES
10953  |  TOMM34  |  DISEASES
60598  |  KCNK15  |  DISEASES
10904  |  BLCAP  |  DISEASES
3065  |  HDAC1  |  DISEASES
2516  |  NR5A1  |  DISEASES
29119  |  CTNNA3  |  DISEASES
164091  |  PAQR7  |  DISEASES
10471  |  PFDN6  |  DISEASES
367  |  AR  |  DISEASES
5081  |  PAX7  |  DISEASES
727837  |  SSX2B  |  DISEASES
79670  |  ZCCHC6  |  DISEASES
7091  |  TLE4  |  DISEASES
2623  |  GATA1  |  DISEASES
3105  |  HLA-A  |  DISEASES
1471  |  CST3  |  DISEASES
56998  |  CTNNBIP1  |  DISEASES
2512  |  FTL  |  DISEASES
3604  |  TNFRSF9  |  DISEASES
22894  |  DIS3  |  DISEASES
22894  |  DIS3  |  DISEASES
4609  |  MYC  |  DISEASES
8516  |  ITGA8  |  DISEASES
5420  |  PODXL  |  DISEASES
4868  |  NPHS1  |  DISEASES
190  |  NR0B1  |  DISEASES
5080  |  PAX6  |  DISEASES
9308  |  CD83  |  DISEASES
2308  |  FOXO1  |  DISEASES
10346  |  TRIM22  |  DISEASES
54790  |  TET2  |  DISEASES
5931  |  RBBP7  |  DISEASES
675  |  BRCA2  |  DISEASES
284390  |  ZNF763  |  DISEASES
4676  |  NAP1L4  |  DISEASES
2296  |  FOXC1  |  DISEASES
1045  |  CDX2  |  DISEASES
2971  |  GTF3A  |  DISEASES
4267  |  CD99  |  DISEASES
2315  |  MLANA  |  DISEASES
6150  |  MRPL23  |  DISEASES
23600  |  AMACR  |  DISEASES
7260  |  TSSC1  |  DISEASES
2254  |  FGF9  |  DISEASES
10232  |  MSLN  |  DISEASES
6736  |  SRY  |  DISEASES
57721  |  METTL14  |  DISEASES
6833  |  ABCC8  |  DISEASES
5077  |  PAX3  |  DISEASES
5973  |  RENBP  |  DISEASES
3161  |  HMMR  |  DISEASES
11346  |  SYNPO  |  DISEASES
2719  |  GPC3  |  DISEASES
2719  |  GPC3  |  DISEASES
10575  |  CCT4  |  DISEASES
10265  |  IRX5  |  DISEASES
5532  |  PPP3CB  |  DISEASES
23475  |  QPRT  |  DISEASES
174  |  AFP  |  DISEASES
115560  |  ZNF501  |  DISEASES
4629  |  MYH11  |  DISEASES
2120  |  ETV6  |  DISEASES
1781  |  DYNC1I2  |  DISEASES
23532  |  PRAME  |  DISEASES
1607  |  DGKB  |  DISEASES
11281  |  POU6F2  |  DISEASES
22976  |  PAXIP1  |  DISEASES
23414  |  ZFPM2  |  DISEASES
56903  |  PAPOLB  |  DISEASES
333932  |  HIST2H3A  |  DISEASES
758  |  MPPED1  |  DISEASES
4435  |  CITED1  |  DISEASES
131578  |  LRRC15  |  DISEASES
55900  |  ZNF302  |  DISEASES
3481  |  IGF2  |  DISEASES
3481  |  IGF2  |  DISEASES
2674  |  GFRA1  |  DISEASES
7849  |  PAX8  |  DISEASES
5076  |  PAX2  |  DISEASES
960  |  CD44  |  DISEASES
3491  |  CYR61  |  DISEASES
23161  |  SNX13  |  DISEASES
2130  |  EWSR1  |  DISEASES
79872  |  CBLL1  |  DISEASES
862  |  RUNX1T1  |  DISEASES
5087  |  PBX1  |  DISEASES
57862  |  ZNF410  |  DISEASES
2668  |  GDNF  |  DISEASES
1028  |  CDKN1C  |  DISEASES
1028  |  CDKN1C  |  DISEASES
80319  |  CXXC4  |  DISEASES
55635  |  DEPDC1  |  DISEASES
627  |  BDNF  |  DISEASES
9391  |  CIAO1  |  DISEASES
5447  |  POR  |  DISEASES
339318  |  ZNF181  |  DISEASES
4750  |  NEK1  |  DISEASES
3347  |  HTN3  |  DISEASES
92312  |  MEX3A  |  DISEASES
5003  |  SLC22A18AS  |  DISEASES
3939  |  LDHA  |  DISEASES
1961  |  EGR4  |  DISEASES
567  |  B2M  |  DISEASES
2297  |  FOXD1  |  DISEASES
9294  |  S1PR2  |  DISEASES
283120  |  H19  |  DISEASES
51214  |  IGF2-AS  |  DISEASES
10984  |  KCNQ1OT1  |  DISEASES
10408  |  MYCNOS  |  DISEASES
6023  |  RMRP  |  DISEASES
6029  |  RN7SL1  |  DISEASES
6029  |  RN7SL1  |  DISEASES
51352  |  WT1-AS  |  DISEASES
Locus(Waiting for update.)
Disease ID 169
Disease wilms tumor
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:1)
HP:0002667  |  Wilms tumor
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:24)
HP:0002664  |  Neoplasia  |  6
HP:0000110  |  Renal dysplasia  |  1
HP:0001399  |  Liver failure  |  1
HP:0001009  |  Telangiectases  |  1
HP:0005584  |  Renal cell carcinoma  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0009733  |  Glioma  |  1
HP:0004448  |  Fulminant hepatic failure  |  1
HP:0030731  |  Carcinoma  |  1
HP:0007281  |  Developmental stagnation  |  1
HP:0006254  |  Increased serum alpha-fetoprotein  |  1
HP:0001520  |  Birthweight > 90th percentile  |  1
HP:0001959  |  Polydipsia  |  1
HP:0001251  |  Ataxia  |  1
HP:0006744  |  Adrenal carcinoma  |  1
HP:0100880  |  Nephrogenic rest  |  1
HP:0003006  |  Neuroblastoma  |  1
HP:0001578  |  Hypercortisolism  |  1
HP:0003774  |  End-stage renal failure  |  1
HP:0001943  |  Hypoglycemia  |  1
HP:0006765  |  Chondrosarcoma  |  1
HP:0001909  |  Leukemia  |  1
HP:0000103  |  Polyuria  |  1
HP:0001903  |  Anemia  |  1
Disease ID 169
Disease wilms tumor
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
C0002793  |  anaplasia  |  4
C0950121  |  drash syndrome  |  1
C0022661  |  end stage renal disease  |  1
C0085602  |  polydipsia  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:14)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1051266255364374524MTHFRumls:C0027708BeFreeThe aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 rs1051266 (G80A) genotypes with the risk of developing nephroblastoma and neuroblastoma.0.0029099162015SLC19A12145537880TC
rs16754211893907490WT1umls:C0027708BeFreeTo analyze the prevalence and clinical implications of Wilms' tumor 1 (WT1) single nucleotide polymorphism (SNP) rs16754 in the context of other prognostic markers in pediatric acute myeloid leukemia (AML).0.4440982872011WT11132396399TC
rs16754216593577490WT1umls:C0027708BeFreeClinical outcome and gene- and microRNA-expression profiling according to the Wilms tumor 1 (WT1) single nucleotide polymorphism rs16754 in adult de novo cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study.0.4440982872011WT11132396399TC
rs1801133255364374524MTHFRumls:C0027708BeFreeThe aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 rs1051266 (G80A) genotypes with the risk of developing nephroblastoma and neuroblastoma.0.0029099162015MTHFR111796321GA
rs2234584151507757490WT1umls:C0027708UNIPROTTwenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development.0.4440982872004WT11132428521GT,A
rs2283873225443646948TCN2umls:C0027708GWASCATA genome-wide association study identifies susceptibility loci for Wilms tumor.0.122012TCN22230617309GA
rs249547822544364255738PCSK9umls:C0027708GWASCATA genome-wide association study identifies susceptibility loci for Wilms tumor.0.122012PCSK9155047322GA
rs2857461217931872130EWSR1umls:C0027708BeFreeOne SNP in EWSR1 (rs2857461) showed a low level of statistical association with the diagnosis of Ewing sarcoma compared to Wilms tumor.0.0024429772012EWSR12229272015CT
rs368087026255364374524MTHFRumls:C0027708BeFreeThe aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 rs1051266 (G80A) genotypes with the risk of developing nephroblastoma and neuroblastoma.0.0029099162015SLC19A12145530890GA
rs3755132225443641653DDX1umls:C0027708GWASCATA genome-wide association study identifies susceptibility loci for Wilms tumor.0.122012DDX1215589696TG
rs386514057255364374524MTHFRumls:C0027708BeFreeThe aim of this study was to investigate the association between MTHFR rs1801133 (C677T) and RFC-1 rs1051266 (G80A) genotypes with the risk of developing nephroblastoma and neuroblastoma.0.0029099162015NANANANANA
rs5955543225443644810NHSumls:C0027708GWASCATA genome-wide association study identifies susceptibility loci for Wilms tumor.0.122012NHSX17680277AG
rs662249725705444PON1umls:C0027708BeFreeThe presence of at least one variant PON1 rs662 R allele increased the risk of developing Wilms´ Tumor although without statistical power.0.0002714422014PON1795308134TC
rs790356225443641740DLG2umls:C0027708GWASCATA genome-wide association study identifies susceptibility loci for Wilms tumor.0.122012DLG2;LOC1053694181183909744AG
GWASdb Annotation(Total Genotypes:8)
Chr Pos SNP_Id RefGene EnsemblGene ENCODE_Factor ENCODE_TFBS Chromosome_interaction GTEx_eQTL SNP_TFBS_affinity_GWAS3D SNP_miRNA_target_affinity_PolymiRTS SNP_splicing_effect_Skippy SNP_splicing_effect_MutPred_Splice SNP_ns_protein_effect_dbNSFP SNP_syn_effect_Silva SNP_phosphorylation_effect_PhosSNP PhastCons_score PhyloP_score GERP++_RS Segway_state Ancestral_allele ESP_AF ESP_AFR ESP_AFR ESP_EUR TG_ASN TG_AMR TG_AFR TG_EUR Type Consequence bStatistic EncH3K27Ac EncH3K4Me1 EncH3K4Me3 EncNucleo OMIM Clinvar
1132410380rs5030316NM_001198551,WT1NM_001198552,WT1NM_000378,WT1NM_024424,WT1NM_024426,WT1ENST00000448076,ENSG00000184937ENST00000332351,ENSG00000184937ENST00000379077,ENSG00000184937ENST00000379079,ENSG00000184937ENST00000530998,ENSG00000184937ENST00000452863,ENSG00000184937ENST00000527882,ENSG00000184937ENST00000527201,ENSG00000254922ENST00000524721,ENSG00000254611ENST00000526998,ENSG00000254439TFP.EBF1NAchr11,32410001,32420000,chr11,32430001,32440000,25,Hi-Cchr11,32410001,32420000,chr11,30250001,30260000,4,Hi-CNALM7,1.3875LM9,1.6073LM19,1.3438LM23,1.543LM64,4.5093hsa-miR-6746-3p,-0.276000NANANANANA0.0080.3172.02GM0
1132411240rs5030310NM_001198551,WT1NM_001198552,WT1NM_000378,WT1NM_024424,WT1NM_024426,WT1ENST00000448076,ENSG00000184937ENST00000332351,ENSG00000184937ENST00000379077,ENSG00000184937ENST00000379079,ENSG00000184937ENST00000530998,ENSG00000184937ENST00000452863,ENSG00000184937ENST00000527882,ENSG00000184937ENST00000527201,ENSG00000254922ENST00000524721,ENSG00000254611ENST00000526998,ENSG00000254439TFP.EBF1NAchr11,32410001,32420000,chr11,32430001,32440000,25,Hi-Cchr11,32410001,32420000,chr11,30250001,30260000,4,Hi-CNALM12,1.9437LM96,1.6012LM175,4.4172LM180,2.5323LM203,2.1185NANANANANANA0.0040.7312.25GE1
1132416875rs5030281NM_001198551,WT1NM_001198552,WT1NM_000378,WT1NM_024424,WT1NM_024426,WT1ENST00000448076,ENSG00000184937ENST00000332351,ENSG00000184937ENST00000379077,ENSG00000184937ENST00000379079,ENSG00000184937ENST00000530998,ENSG00000184937ENST00000452863,ENSG00000184937ENST00000527882,ENSG00000184937ENST00000527201,ENSG00000254922ENST00000524721,ENSG00000254611ENST00000526998,ENSG00000254439ENST00000526685,ENSG00000184937TFP.CTCFTFP.RAD21MCV-4NAchr11,32410001,32420000,chr11,32430001,32440000,25,Hi-Cchr11,32410001,32420000,chr11,30250001,30260000,4,Hi-CNALM203,1.3929FOXF2,45.4838Foxd3,3.791Foxa2,10.0622PPARG-RXRA,1.2759NANANANANANA0.000
1132423752rs5030244NM_001198551,WT1NM_001198552,WT1NM_000378,WT1NM_024424,WT1NM_024426,WT1ENST00000448076,ENSG00000184937ENST00000332351,ENSG00000184937ENST00000379077,ENSG00000184937ENST00000379079,ENSG00000184937ENST00000530998,ENSG00000184937ENST00000452863,ENSG00000184937ENST00000527882,ENSG00000184937ENST00000527201,ENSG00000254922ENST00000524721,ENSG00000254611ENST00000526998,ENSG00000254439ENST00000527775,ENSG00000184937NANANANABarx1_2877,2.7215Barx2_3447,1.3938Cdx2_4272,1.3316Hmx1_3423,10.0742Hmx2_3424,10.7379NANANANANANA0.0132.0253.78GE0
1132435529rs2900740NM_001198551,WT1NM_001198552,WT1NM_000378,WT1NM_024424,WT1NM_024426,WT1ENST00000448076,ENSG00000184937ENST00000332351,ENSG00000184937ENST00000379077,ENSG00000184937ENST00000379079,ENSG00000184937ENST00000530998,ENSG00000184937ENST00000452863,ENSG00000184937ENST00000527882,ENSG00000184937ENST00000527201,ENSG00000254922ENST00000524721,ENSG00000254611ENST00000526998,ENSG00000254439ENST00000527775,ENSG00000184937MCV-1NAchr11,32430001,32440000,chr11,32410001,32420000,25,Hi-CNANANANANANANANA0.000-1.153-4.98GE1GNANANA
1132446985rs12293750NM_001198551,WT1NM_001198552,WT1NM_000378,WT1NM_024424,WT1NM_024426,WT1ENST00000448076,ENSG00000184937ENST00000332351,ENSG00000184937ENST00000379077,ENSG00000184937ENST00000379079,ENSG00000184937ENST00000530998,ENSG00000184937ENST00000452863,ENSG00000184937ENST00000527201,ENSG00000254922ENST00000524721,ENSG00000254611ENST00000526998,ENSG00000254439ENST00000527775,ENSG00000184937MCV-11NAchr11,32440001,32450000,chr22,17040001,17050000,25,Hi-CNALM11,2.9255LM51,1.7867LM60,1.7067LM72,1.7266LM81,13.0445NANANANANANA0.0050.4561.61R4C
1132447347rs7110547NM_001198551,WT1NM_001198552,WT1NM_000378,WT1NM_024424,WT1NM_024426,WT1ENST00000448076,ENSG00000184937ENST00000332351,ENSG00000184937ENST00000379077,ENSG00000184937ENST00000379079,ENSG00000184937ENST00000530998,ENSG00000184937ENST00000452863,ENSG00000184937ENST00000527201,ENSG00000254922ENST00000524721,ENSG00000254611ENST00000526998,ENSG00000254439ENST00000527775,ENSG00000184937MCV-6NAchr11,32440001,32450000,chr22,17040001,17050000,25,Hi-CNALM12,4.2671LM25,1.3006LM25,1.3006LM162,3.3264LM170,2.1769NANANANANANA0.0020.5091.35GE0G
1132455527rs3930513NM_000378,WT1NM_024424,WT1NM_024426,WT1ENST00000448076,ENSG00000184937ENST00000332351,ENSG00000184937ENST00000379077,ENSG00000184937ENST00000452863,ENSG00000184937ENST00000527201,ENSG00000254922ENST00000524721,ENSG00000254611ENST00000526998,ENSG00000254439TFP.SUZ12TFP.TAF1TFP.TBPTFP.E2F6TFP.MYCTFP.YY1TFP.MAXTFP.SIN3ATFP.CTBP2TFP.EGR1TFP.SPI1TFP.ZBTB7ATFP.HDAC2MCV-10NAchr11,32450001,32460000,chr3,145640001,145650000,25,Hi-Cchr11,32450001,32460000,chr7,101970001,101980000,29,Hi-CNALM231,2.1728Pax5,1.4414GATA-1,2.2919AhR,3.8792LUN-1,2.4693NANA
GWASdb Snp Trait(Total Genotypes:51)
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
155512995rs2495478GArs2495478225443641.00E-07NA1.4[1.15-1.72] 757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomars2495478-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCPCSK9
215729820rs3755132TGrs3755132225443641.00E-14NA1.45[1.29-1.64]757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomars3755132-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGNA
215737343rs2302930AGrs2302930225443643.10E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tADDX1
215737480rs2302931CArs2302931225443643.10E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCDDX1
215750443rs4668942TCrs4668942225443643.10E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTDDX1
215750640rs7594193AGrs7594193225443643.10E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGDDX1
215758293rs3770466TCrs3770466225443643.10E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCDDX1
215762935rs3770467GArs3770467225443643.14E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGDDX1
215763788rs41264163CTrs41264163225443643.14E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTDDX1
215764078rs4668945GCrs4668945225443643.34E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGDDX1
215765425rs6734471CTrs6734471225443643.34E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCDDX1
215767761rs6743036GArs6743036225443643.34E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tNADDX1
215768256rs6743630GArs6743630225443643.34E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tADDX1
215770507rs3770470GTrs3770470225443643.34E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTDDX1
215770775rs3770471CTrs3770471225443643.34E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCDDX1
215771586rs4668948ACrs4668948225443642.55E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tANA
215771615rs4668949CTrs4668949225443641.51E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTNA
215772546rs976015CGrs976015225443643.14E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCNA
215772958rs16862822GArs16862822225443643.34E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGNA
215774115rs976233CTrs976233225443643.34E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCNA
215775210rs16862823TCrs16862823225443643.14E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTNA
215782471rs807624GTrs807624225443641.00E-14NA1.33[1.22-1.45]757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomars807624-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tANA
215786243rs6724800AGrs6724800225443641.86E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tANA
215788191rs16862838CTrs16862838225443641.71E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCNA
215789441rs4668458GArs4668458225443642.22E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGNA
215791937rs6431721CTrs6431721225443642.66E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCNA
591845809rs6887553AGrs6887553225443645.35E-10NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGNA
591859029rs10060683TCrs10060683225443642.41E-10NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCNA
591893792rs1027643CTrs1027643225443645.00E-10NA1.43[1.18-1.73]757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomars1027643-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTNA
591904447rs61344503GTrs61344503225443642.40E-10NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTNA
591907006rs2221269AGrs2221269225443641.45E-10NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tANA
1183620787rs790356AGrs790356225443644.00E-15NA1.28[1.17-1.39]757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomars790356-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tADLG2
2231009839rs11913239CTrs11913239225443646.49E-09NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCTCN2
2231010997rs2267162CTrs2267162225443641.12E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCTCN2
2231011280rs7290898AC,G,Trs7290898225443642.97E-09NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCTCN2
2231011923rs16988855TCrs16988855225443645.40E-09NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCTCN2
2231013296rs2283873GArs2283873225443645.00E-12NA2.05[1.57-2.69]757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomars2283873-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCTCN2
2231014377rs2009857CTrs2009857225443645.40E-09NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGTCN2
2231015562rs7288627GArs7288627225443645.40E-09NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGTCN2
2231015573rs7288385CArs7288385225443645.40E-09NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCTCN2
2231018072rs8141515TCrs8141515225443641.17E-08NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTTCN2
2231018078rs2267166GArs2267166225443641.17E-08NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tGTCN2
2231022733rs2072195ATrs2072195225443641.13E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tATCN2
X17669042rs4825280TArs4825280225443642.54E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTNHS
X17677803rs978158ATrs978158225443642.54E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tANHS
X17692151rs6633014CTrs6633014225443642.54E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTNHS
X17693746rs5955717CTrs5955717225443642.54E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tTNHS
X17695190rs5955731CArs5955731225443642.54E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCNHS
X17698397rs5955543AGrs5955543225443641.00E-09NA2.64[1.74-4.01] 757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomars5955543-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tANHS
X17699505rs12392874CArs12392874225443642.54E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tCNHS
X17699834rs4825243CArs4825243225443642.54E-06NANANA757 European ancestry cases; 1,879 European ancestry controlsEuropean(2636)ALL(2636)EUR(2636)ALL(2636)Wilms tumorHPOID:0002667Nephroblastoma (Wilms tumor)DOID:2154nephroblastomaD009396Wilms TumornephroblastomaNephroblastomaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tANHS
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:8)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0027708carbamazepineD002220298-46-4wilms tumorMESH:D009396marker/mechanism6106127
C0027708cisplatinD00294515663-27-1wilms tumorMESH:D009396therapeutic2206854
C0027708ifosfamideD0070693778-73-2wilms tumorMESH:D009396therapeutic2166154
C0027708melphalanD008558148-82-3wilms tumorMESH:D009396therapeutic15591903
C0027708phenytoinD01067257-41-0wilms tumorMESH:D009396marker/mechanism6106127
C0027708tretinoinD014212302-79-4wilms tumorMESH:D009396therapeutic16287080
C0027708vincristineD014750-wilms tumorMESH:D009396therapeutic15838404
C0027708vindesineD01475153643-48-4wilms tumorMESH:D009396therapeutic455587
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)