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rs863225378

From SNPedia

ClinVar
Risk rs863225378(ATCTGGACC;ATCTGGACC)
Alt rs863225378(ATCTGGACC;ATCTGGACC)
Reference rs863225378(GG;GG)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MLH1
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.37089068_37089069delGGinsATCTGGACC
CLNSRC
CLNACC RCV000202288.1, RCV000218337.1,