Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs776935407
rs776935407
CUI: C0025202
Disease: melanoma
melanoma
0.010 GeneticVariation BEFREE Additional studies of BRAF have demonstrated that the T1799A mutation is absent in uveal melanomas and Spitz nevi. 15811117

2005