ClinVar Miner

List of variants in gene APOB reported as uncertain significance by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.11761G>A (p.Val3921Ile) rs72654409 0.00234
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser) rs72653077 0.00198
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr) rs72653092 0.00061
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu) rs41288783 0.00058
NM_000384.3(APOB):c.10672C>T (p.Arg3558Cys) rs12713559 0.00050
NM_000384.3(APOB):c.9639C>A (p.Asn3213Lys) rs574725520 0.00025
NM_000384.3(APOB):c.5599C>T (p.Arg1867Trp) rs200583769 0.00024
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met) rs148498577 0.00024
NM_000384.3(APOB):c.10708C>T (p.His3570Tyr) rs201736972 0.00019
NM_000384.3(APOB):c.13181T>C (p.Val4394Ala) rs12720843 0.00017
NM_000384.3(APOB):c.2258G>A (p.Gly753Glu) rs148502464 0.00013
NM_000384.3(APOB):c.2914G>A (p.Gly972Ser) rs199893862 0.00013
NM_000384.3(APOB):c.6655C>T (p.Arg2219Cys) rs141641980 0.00007
NM_000384.3(APOB):c.7698G>C (p.Glu2566Asp) rs149306841 0.00007
NM_000384.3(APOB):c.7853T>C (p.Ile2618Thr) rs531273434 0.00003
NM_000384.3(APOB):c.13154G>A (p.Arg4385His) rs533755016 0.00001
NM_000384.3(APOB):c.10556C>T (p.Thr3519Ile) rs746951119

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