ClinVar Miner

List of variants in gene APOB reported as uncertain significance by Division of Genomic Diagnostics,The Children's Hospital of Philadelphia

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Total variants: 14
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HGVS dbSNP
NM_000384.3(APOB):c.12766G>A (p.Glu4256Lys) rs61743313
NM_000384.3(APOB):c.1310G>A (p.Arg437His) rs142114415
NM_000384.3(APOB):c.13153C>T (p.Arg4385Cys) rs864309556
NM_000384.3(APOB):c.3337G>C (p.Asp1113His) rs12713844
NM_000384.3(APOB):c.3362A>G (p.Lys1121Arg) rs879255342
NM_000384.3(APOB):c.3670C>T (p.Arg1224Trp) rs148959244
NM_000384.3(APOB):c.3724T>A (p.Ser1242Thr) rs200261177
NM_000384.3(APOB):c.4027C>T (p.Pro1343Ser) rs374427541
NM_000384.3(APOB):c.4178C>T (p.Ala1393Val) rs143282164
NM_000384.3(APOB):c.574G>A (p.Val192Ile) rs200662943
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr) rs72653092
NM_000384.3(APOB):c.7721C>T (p.Ala2574Val) rs150843941
NM_000384.3(APOB):c.8462C>T (p.Pro2821Leu) rs72653095
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly) rs12720854

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