Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1064794292
rs1064794292
CUI: C0025202
Disease: melanoma
melanoma
0.710 GeneticVariation BEFREE We detected the p.Gly23Asp missense mutation in one of the two tested melanoma patients of a family with three melanoma cases. 19712690

2009