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rs876659098

From SNPedia

ClinVar
Risk rs876659098(CAGGTCAGGACATCCA;CAGGTCAGGACATCCA)
Alt rs876659098(CAGGTCAGGACATCCA;CAGGTCAGGACATCCA)
Reference rs876659098(ACACT;ACACT)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TP53
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.7577511_7577515delAGTGTinsTGGATGTCCTGACCTG
CLNSRC
CLNACC RCV000219279.1,