WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121907900
rs121907900
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C1837026
Disease:
MEACHAM SYNDROME (disorder)
A 0.700 CausalMutation CLINVAR
dbSNP: rs121907906
rs121907906
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C1837026
Disease:
MEACHAM SYNDROME (disorder)
A 0.700 CausalMutation CLINVAR
dbSNP: rs121907910
rs121907910
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C1837026
Disease:
MEACHAM SYNDROME (disorder)
A 0.700 CausalMutation CLINVAR