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rs863225421

From SNPedia

ClinVar
Risk rs863225421(G;G)
Alt rs863225421(G;G)
Reference rs863225421(;)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48026022dupG
CLNSRC
CLNACC RCV000202094.1, RCV000213447.1,