rs1554939839, WT1

N. diseases: 4
Disease: WAGR Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
WAGR Syndrome
CUI: C0206115
Disease: WAGR Syndrome
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