ClinVar Miner

List of variants in gene APOB reported as likely benign by PreventionGenetics

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Total variants: 11
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HGVS dbSNP
NM_000384.2(APOB):c.11244G>A (p.Thr3748=) rs72654406
NM_000384.2(APOB):c.13441G>A (p.Ala4481Thr) rs1801695
NM_000384.2(APOB):c.1594C>T (p.Arg532Trp) rs13306194
NM_000384.2(APOB):c.293C>T (p.Thr98Ile) rs1367117
NM_000384.2(APOB):c.3122-6G>A rs72653071
NM_000384.2(APOB):c.3337G>C (p.Asp1113His) rs12713844
NM_000384.2(APOB):c.7152T>C (p.Val2384=) rs72653090
NM_000384.2(APOB):c.7612C>T (p.Leu2538=) rs72653093
NM_000384.2(APOB):c.7696G>A (p.Glu2566Lys) rs1801696
NM_000384.2(APOB):c.7998A>G (p.Val2666=) rs1042006
NM_000384.2(APOB):c.8462C>T (p.Pro2821Leu) rs72653095

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