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rs876659310

From SNPedia

ClinVar
Risk rs876659310(TTT;TTT)
Alt rs876659310(TTT;TTT)
Reference rs876659310(AGAATCCAGAAGGCCTTTC;AGAATCCAGAAGGCCTTTC)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41228571_41228589del19insAAA
CLNSRC
CLNACC RCV000216050.1,