WNT5A, Wnt family member 5A, 7474

N. diseases: 375; N. variants: 11
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906663
rs387906663
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		0.800 GeneticVariation UNIPROT WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010
dbSNP: rs387906663
rs387906663
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		G 0.800 CausalMutation CLINVAR