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rs876658865

From SNPedia

ClinVar
Risk rs876658865(T;T)
Alt rs876658865(T;T)
Reference rs876658865(CCC;CCC)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000016.9:g.68772275_68772277delCCCinsT
CLNSRC
CLNACC RCV000215517.1,