ClinVar Miner

List of variants reported as uncertain significance for 3-hydroxy-3-methylglutaryl-CoA synthase deficiency by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_005518.4(HMGCS2):c.347G>A (p.Arg116His) rs147906427 0.00021
NM_005518.4(HMGCS2):c.953A>G (p.Asn318Ser) rs766507770 0.00020
NM_005518.4(HMGCS2):c.241G>A (p.Ala81Thr) rs151187711 0.00019
NM_005518.4(HMGCS2):c.274C>G (p.Arg92Gly) rs771955824 0.00018
NM_005518.4(HMGCS2):c.73C>G (p.Pro25Ala) rs144744634 0.00016
NM_005518.4(HMGCS2):c.1153T>A (p.Ser385Thr) rs4716 0.00015
NM_005518.4(HMGCS2):c.894G>A (p.Met298Ile) rs138086607 0.00012
NM_005518.4(HMGCS2):c.358C>A (p.Pro120Thr) rs758033248 0.00011
NM_005518.4(HMGCS2):c.8G>A (p.Arg3His) rs72695184 0.00011
NM_005518.4(HMGCS2):c.586G>C (p.Asp196His) rs149314406 0.00010
NM_005518.4(HMGCS2):c.146C>T (p.Thr49Ile) rs756404916 0.00009
NM_005518.4(HMGCS2):c.71C>T (p.Thr24Ile) rs369221781 0.00009
NM_005518.4(HMGCS2):c.275G>A (p.Arg92His) rs144921290 0.00007
NM_005518.4(HMGCS2):c.790C>T (p.Arg264Trp) rs773945291 0.00007
NM_005518.4(HMGCS2):c.364G>A (p.Asp122Asn) rs368014391 0.00006
NM_005518.4(HMGCS2):c.803G>A (p.Arg268Gln) rs371306326 0.00006
NM_005518.4(HMGCS2):c.1289C>T (p.Ala430Val) rs141769037 0.00005
NM_005518.4(HMGCS2):c.502G>A (p.Gly168Ser) rs746217014 0.00005
NM_005518.4(HMGCS2):c.35T>A (p.Leu12Gln) rs939049952 0.00004
NM_005518.4(HMGCS2):c.50C>T (p.Ala17Val) rs587712415 0.00004
NM_005518.4(HMGCS2):c.595G>A (p.Val199Ile) rs150140061 0.00004
NM_005518.4(HMGCS2):c.105-3C>T rs1035647830 0.00003
NM_005518.4(HMGCS2):c.1513C>T (p.Arg505Trp) rs780044819 0.00003
NM_005518.4(HMGCS2):c.791G>A (p.Arg264Gln) rs372095379 0.00003
NM_005518.4(HMGCS2):c.880G>A (p.Asp294Asn) rs144103604 0.00003
NM_005518.4(HMGCS2):c.1127C>T (p.Thr376Ile) rs772359110 0.00002
NM_005518.4(HMGCS2):c.1220T>C (p.Ile407Thr) rs766898190 0.00002
NM_005518.4(HMGCS2):c.346C>T (p.Arg116Cys) rs200607527 0.00002
NM_005518.4(HMGCS2):c.695G>T (p.Gly232Val) rs1002548815 0.00002
NM_005518.4(HMGCS2):c.830T>A (p.Ile277Asn) rs775637086 0.00002
NM_005518.4(HMGCS2):c.940C>T (p.Arg314Cys) rs781567781 0.00002
NM_005518.4(HMGCS2):c.1082A>G (p.Gln361Arg) rs1286357569 0.00001
NM_005518.4(HMGCS2):c.1175C>T (p.Ser392Leu) rs766097440 0.00001
NM_005518.4(HMGCS2):c.1271G>A (p.Arg424Gln) rs748252959 0.00001
NM_005518.4(HMGCS2):c.1405C>G (p.Gln469Glu) rs754218759 0.00001
NM_005518.4(HMGCS2):c.1451G>T (p.Ser484Ile) rs763005476 0.00001
NM_005518.4(HMGCS2):c.160G>A (p.Val54Met) rs28937320 0.00001
NM_005518.4(HMGCS2):c.743C>T (p.Ser248Leu) rs768912442 0.00001
NM_005518.4(HMGCS2):c.88C>G (p.Pro30Ala) rs202069145 0.00001
NM_005518.4(HMGCS2):c.1015G>A (p.Gly339Arg)
NM_005518.4(HMGCS2):c.1015G>T (p.Gly339Trp) rs775277893
NM_005518.4(HMGCS2):c.103A>G (p.Arg35Gly) rs1653321576
NM_005518.4(HMGCS2):c.1046A>G (p.Asn349Ser) rs1025175254
NM_005518.4(HMGCS2):c.104G>T (p.Arg35Met) rs751101083
NM_005518.4(HMGCS2):c.1078T>G (p.Ser360Ala) rs1286992834
NM_005518.4(HMGCS2):c.1093G>A (p.Asp365Asn)
NM_005518.4(HMGCS2):c.1095C>G (p.Asp365Glu) rs587690380
NM_005518.4(HMGCS2):c.1112C>G (p.Ser371Cys)
NM_005518.4(HMGCS2):c.1118A>C (p.Tyr373Ser) rs1652805414
NM_005518.4(HMGCS2):c.1142T>G (p.Met381Arg) rs771289268
NM_005518.4(HMGCS2):c.1156C>A (p.Leu386Met)
NM_005518.4(HMGCS2):c.1256G>A (p.Ser419Asn)
NM_005518.4(HMGCS2):c.1262T>G (p.Phe421Cys) rs1652723339
NM_005518.4(HMGCS2):c.1316T>C (p.Val439Ala)
NM_005518.4(HMGCS2):c.1355G>A (p.Arg452Gln) rs770800317
NM_005518.4(HMGCS2):c.1372G>A (p.Glu458Lys)
NM_005518.4(HMGCS2):c.1498C>T (p.Arg500Cys)
NM_005518.4(HMGCS2):c.1514G>A (p.Arg505Gln)
NM_005518.4(HMGCS2):c.158A>G (p.Asp53Gly)
NM_005518.4(HMGCS2):c.182T>G (p.Val61Gly)
NM_005518.4(HMGCS2):c.205G>A (p.Asp69Asn)
NM_005518.4(HMGCS2):c.245G>A (p.Gly82Glu) rs1653149765
NM_005518.4(HMGCS2):c.279G>A (p.Met93Ile) rs1557994090
NM_005518.4(HMGCS2):c.28C>A (p.Arg10Ser)
NM_005518.4(HMGCS2):c.334C>T (p.Arg112Trp)
NM_005518.4(HMGCS2):c.412T>C (p.Ser138Pro) rs764209022
NM_005518.4(HMGCS2):c.428C>G (p.Thr143Arg) rs760689678
NM_005518.4(HMGCS2):c.533A>G (p.Asn178Ser) rs1386957244
NM_005518.4(HMGCS2):c.540G>T (p.Met180Ile) rs1161245291
NM_005518.4(HMGCS2):c.560-3C>T rs1652986854
NM_005518.4(HMGCS2):c.56A>G (p.Gln19Arg) rs2101283600
NM_005518.4(HMGCS2):c.589A>G (p.Ile197Val) rs2101263939
NM_005518.4(HMGCS2):c.605G>A (p.Ser202Asn)
NM_005518.4(HMGCS2):c.704T>C (p.Met235Thr) rs773806829
NM_005518.4(HMGCS2):c.705G>A (p.Met235Ile) rs2101262597
NM_005518.4(HMGCS2):c.73C>T (p.Pro25Ser) rs144744634
NM_005518.4(HMGCS2):c.754A>G (p.Ile252Val)
NM_005518.4(HMGCS2):c.797T>C (p.Leu266Ser)
NM_005518.4(HMGCS2):c.79C>T (p.Arg27Cys)
NM_005518.4(HMGCS2):c.814T>C (p.Ser272Pro) rs1571037413
NM_005518.4(HMGCS2):c.851C>G (p.Ala284Gly)
NM_005518.4(HMGCS2):c.866C>A (p.Pro289His) rs146296049
NM_005518.4(HMGCS2):c.874C>A (p.Leu292Ile) rs769844821
NM_005518.4(HMGCS2):c.887A>C (p.Gln296Pro)
NM_005518.4(HMGCS2):c.941G>A (p.Arg314His)
NM_005518.4(HMGCS2):c.973A>G (p.Ser325Gly)

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