WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Disease: WAGR Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554939839
rs1554939839
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C0206115
Disease:
WAGR Syndrome 		C 0.700 CausalMutation CLINVAR Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development. 15150775 2004