WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Disease: NEPHROTIC SYNDROME, TYPE 4 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776576
rs587776576
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		T 0.700 CausalMutation CLINVAR Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development. 1302008 1992
dbSNP: rs1037084691
rs1037084691
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121907900
rs121907900
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121907906
rs121907906
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1554939785
rs1554939785
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs28941777
rs28941777
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		G 0.700 CausalMutation CLINVAR
dbSNP: rs28941778
rs28941778
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs28941778
rs28941778
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		T 0.700 CausalMutation CLINVAR
dbSNP: rs28942089
rs28942089
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		A 0.700 CausalMutation CLINVAR
dbSNP: rs587776577
rs587776577
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C3151568
Disease:
NEPHROTIC SYNDROME, TYPE 4 		A 0.700 CausalMutation CLINVAR