WNT5A, Wnt family member 5A, 7474

N. diseases: 375; N. variants: 11
Disease: Congenital Abnormality ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs524153
rs524153
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0000768
Disease:
Congenital Abnormality 		0.010 GeneticVariation BEFREE Individuals carrying a homozygous genotype CC (rs524153) or GG (rs504849) had a similarly reduced risk of conotruncal malformations. 26278011 2015