ClinVar Miner

List of variants in gene APOB reported as uncertain significance by Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 18
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NM_000384.3(APOB):c.10556C>T (p.Thr3519Ile) rs746951119
NM_000384.3(APOB):c.10672C>T (p.Arg3558Cys)
NM_000384.3(APOB):c.10708C>T (p.His3570Tyr) rs201736972
NM_000384.3(APOB):c.11761G>A (p.Val3921Ile)
NM_000384.3(APOB):c.13154G>A (p.Arg4385His) rs533755016
NM_000384.3(APOB):c.13181T>C (p.Val4394Ala) rs12720843
NM_000384.3(APOB):c.13288T>A (p.Ser4430Thr) rs72654426
NM_000384.3(APOB):c.2914G>A (p.Gly972Ser) rs199893862
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu)
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser)
NM_000384.3(APOB):c.5066G>A (p.Arg1689His)
NM_000384.3(APOB):c.5599C>T (p.Arg1867Trp) rs200583769
NM_000384.3(APOB):c.6655C>T (p.Arg2219Cys) rs141641980
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr)
NM_000384.3(APOB):c.7698G>C (p.Glu2566Asp) rs149306841
NM_000384.3(APOB):c.7853T>C (p.Ile2618Thr) rs531273434
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met) rs148498577
NM_000384.3(APOB):c.9639C>A (p.Asn3213Lys) rs574725520

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