Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659098

From SNPedia

ClinVar
Risk rs876659098(CAGGTCAGGACATCCA;CAGGTCAGGACATCCA)
Alt rs876659098(CAGGTCAGGACATCCA;CAGGTCAGGACATCCA)
Reference Rs876659098(ACACT;ACACT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577511_7577515delAGTGTinsTGGATGTCCTGACCTG
CLNSRC
CLNACC RCV000219279.1,