Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553811652
rs1553811652
Entrez Id: 1857
Gene Symbol: DVL3
DVL3
CUI: C4225363
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2
A 0.700 GeneticVariation CLINVAR