WNT5A, Wnt family member 5A, 7474

N. diseases: 375; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204836
rs786204836
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0265205
Disease:
Robinow Syndrome
C 0.700 CausalMutation CLINVAR De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. 24716670 2015