Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397509413
rs397509413
Entrez Id: 8314;51533
Gene Symbol: BAP1;PHF7
BAP1;PHF7
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
AC 0.700 CausalMutation CLINVAR Hereditary uveal melanoma: a report of a germline mutation in BAP1. 23341325 2013