WNT5A, Wnt family member 5A, 7474

N. diseases: 375; N. variants: 11
Disease: Robinow Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786200925
rs786200925
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0265205
Disease:
Robinow Syndrome 		G 0.700 CausalMutation CLINVAR WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010