ClinVar Miner

List of variants reported as other for not provided

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Total variants: 74
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HGVS dbSNP
CYP2C19*17 rs12248560
CYP2C19*3 rs4986893
CYP2C19*4A rs28399504
CYP2C19*5 rs56337013
CYP2C19*8 rs41291556
CYP2C9*6 rs9332131
CYP2D6*2A
NC_000022.10:g.42523943G>A
NM_000036.2(AMPD1):c.133C>T (p.Gln45Ter) rs17602729
NM_000036.2(AMPD1):c.242C>T (p.Pro81Leu) rs61752479
NM_000041.2(APOE):c.526C>T (p.Arg176Cys) rs7412
NM_000041.4(APOE):c.388T>C (p.Cys130Arg) rs429358
NM_000098.3(CPT2):c.1342T>C (p.Phe448Leu) rs74315297
NM_000104.3(CYP1B1):c.685G>A (p.Glu229Lys) rs57865060
NM_000106.5(CYP2D6):c.*264G>A (p.Gly169Arg)
NM_000106.5(CYP2D6):c.124G>A (p.Gly42Arg)
NM_000106.5(CYP2D6):c.320C>T (p.Thr107Ile)
NM_000106.5(CYP2D6):c.454delT (p.Trp152Glyfs) rs5030655
NM_000106.5(CYP2D6):c.505G>T (p.Gly169Ter) rs5030865
NM_000106.5(CYP2D6):c.506-1G>A rs3892097
NM_000106.5(CYP2D6):c.775delA (p.Arg259Glyfs) rs35742686
NM_000106.5(CYP2D6):c.841_843delAAG (p.Lys281del)
NM_000106.5(CYP2D6):c.971A>C (p.His324Pro)
NM_000106.5(CYP2D6):c.985+39G>A rs28371725
NM_000106.6(CYP2D6):c.100C>T (p.Pro34Ser) rs1065852
NM_000106.6(CYP2D6):c.1012G>A (p.Val338Met)
NM_000106.6(CYP2D6):c.1457G>C (p.Ser486Thr) rs1135840
NM_000131.4(F7):c.1091G>A (p.Arg364Gln) rs121964926
NM_000137.3(FAH):c.1021C>T (p.Arg341Trp) rs11555096
NM_000152.5(GAA):c.271G>A (p.Asp91Asn) rs1800299
NM_000155.2(GALT):c.-119_-116delGTCA rs111033640
NM_000155.4(GALT):c.652C>T (p.Leu218=) rs2070075
NM_000155.4(GALT):c.940A>G (p.Asn314Asp) rs2070074
NM_000157.4(GBA):c.882T>G (p.His294Gln) rs367968666
NM_000169.2(GLA):c.937G>T (p.Asp313Tyr) rs28935490
NM_000203.5(IDUA):c.235G>A (p.Ala79Thr) rs58037052
NM_000203.5(IDUA):c.246C>G (p.His82Gln) rs148775298
NM_000219.6(KCNE1):c.253G>A (p.Asp85Asn) rs1805128
NM_000237.3(LPL):c.106G>A (p.Asp36Asn) rs1801177
NM_000350.3(ABCA4):c.4222T>C (p.Trp1408Arg) rs61750135
NM_000350.3(ABCA4):c.4918C>T (p.Arg1640Trp) rs61751404
NM_000367.4(TPMT):c.460G>A (p.Ala154Thr) rs1800460
NM_000367.4(TPMT):c.719A>G (p.Tyr240Cys) rs1142345
NM_000410.3(HFE):c.187C>G (p.His63Asp) rs1799945
NM_000410.3(HFE):c.845G>A (p.Cys282Tyr) rs1800562
NM_000487.6(ARSA):c.*96A>G rs6151429
NM_000487.6(ARSA):c.1055A>G (p.Asn352Ser) rs2071421
NM_000487.6(ARSA):c.1397C>T (p.Ala466Val) rs763065602
NM_000492.3(CFTR):c.1210-11T>G rs73715573
NM_000520.4(HEXA):c.745C>T (p.Arg249Trp) rs138058578
NM_000520.5(HEXA):c.739C>T (p.Arg247Trp) rs121907970
NM_000521.4(HEXB):c.1627G>A (p.Ala543Thr) rs121907984
NM_000769.1(CYP2C19):c.681G>A (p.Pro227=) rs4244285
NM_000771.3(CYP2C9):c.1075A>C (p.Ile359Leu) rs1057910
NM_000771.3(CYP2C9):c.430C>T (p.Arg144Cys) rs1799853
NM_000771.4(CYP2C9):c.1080C>G (p.Asp360Glu) rs28371686
NM_001008216.2(GALE):c.770A>G (p.Lys257Arg) rs28940884
NM_001008216.2(GALE):c.956G>A (p.Gly319Glu) rs28940885
NM_001072.4(UGT1A6):c.1088C>T (p.Pro363Leu) rs34946978
NM_001072.4(UGT1A6):c.862-6061C>A rs35350960
NM_001072.4(UGT1A6):c.862-6073T>G rs35003977
NM_001072.4(UGT1A6):c.862-6223T>A rs72551341
NM_001072.4(UGT1A6):c.862-6799_862-6798insTA rs1559406508
NM_001127701.1(SERPINA1):c.839A>T (p.Asp280Val) rs121912714
NM_001127701.1(SERPINA1):c.863A>T (p.Glu288Val) rs17580
NM_001370658.1(BTD):c.1147T>G (p.Phe383Val) rs104893686
NM_003742.4(ABCB11):c.3556G>A (p.Glu1186Lys) rs1521808
NM_005957.4(MTHFR):c.1286A>C (p.Glu429Ala) rs1801131
NM_005957.4(MTHFR):c.1781G>A (p.Arg594Gln) rs2274976
NM_005957.4(MTHFR):c.665C>T (p.Ala222Val) rs1801133
NM_006446.5(SLCO1B1):c.521T>C (p.Val174Ala) rs4149056
NM_016579.4(CD320):c.256_258GAG[2] (p.Glu88del) rs150384171
NM_024006.4(VKORC1):c.-1639G>A rs9923231
NM_145870.3(GSTZ1):c.259C>T (p.Arg87Ter) rs747265163

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