ClinVar Miner

List of variants in gene PLOD1 studied for Cardiovascular phenotype

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Total variants: 75
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HGVS dbSNP
NM_000302.4(PLOD1):c.*4G>A rs750397415
NM_000302.4(PLOD1):c.*4G>T rs750397415
NM_000302.4(PLOD1):c.1083C>T (p.Ala361=) rs1159010003
NM_000302.4(PLOD1):c.1098-3C>T rs541901674
NM_000302.4(PLOD1):c.1110G>A (p.Arg370=) rs148644646
NM_000302.4(PLOD1):c.1140C>T (p.Ser380=) rs200131516
NM_000302.4(PLOD1):c.1141G>A (p.Val381Met) rs2230896
NM_000302.4(PLOD1):c.1145A>G (p.Asp382Gly) rs998178222
NM_000302.4(PLOD1):c.1152C>T (p.Asp384=) rs771685198
NM_000302.4(PLOD1):c.1164C>T (p.Thr388=) rs74949176
NM_000302.4(PLOD1):c.1172A>G (p.Asn391Ser) rs763409574
NM_000302.4(PLOD1):c.1203-3C>T rs376288573
NM_000302.4(PLOD1):c.1206C>T (p.Asn402=) rs1130529
NM_000302.4(PLOD1):c.1209C>T (p.Val403=) rs1401528073
NM_000302.4(PLOD1):c.1216C>G (p.Pro406Ala) rs760764359
NM_000302.4(PLOD1):c.124C>T (p.Arg42Cys) rs202003686
NM_000302.4(PLOD1):c.1299C>T (p.Asp433=) rs886039111
NM_000302.4(PLOD1):c.1321C>T (p.Arg441Trp) rs11553676
NM_000302.4(PLOD1):c.1428G>A (p.Lys476=) rs139869965
NM_000302.4(PLOD1):c.1471-2A>G rs1401035675
NM_000302.4(PLOD1):c.1495C>T (p.Arg499Trp) rs149124387
NM_000302.4(PLOD1):c.1533C>G (p.Tyr511Ter) rs121913552
NM_000302.4(PLOD1):c.1534C>T (p.Arg512Cys) rs138490756
NM_000302.4(PLOD1):c.1582G>A (p.Glu528Lys) rs112250644
NM_000302.4(PLOD1):c.1632A>C (p.Ala544=) rs2230898
NM_000302.4(PLOD1):c.166C>T (p.Gln56Ter) rs1433428588
NM_000302.4(PLOD1):c.1670G>C (p.Trp557Ser) rs1052289406
NM_000302.4(PLOD1):c.1685C>T (p.Thr562Met) rs770120389
NM_000302.4(PLOD1):c.177C>T (p.Gly59=) rs34032489
NM_000302.4(PLOD1):c.1788G>T (p.Val596=) rs35460537
NM_000302.4(PLOD1):c.1791G>C (p.Pro597=) rs151051718
NM_000302.4(PLOD1):c.1865C>T (p.Pro622Leu) rs766973023
NM_000302.4(PLOD1):c.1927G>A (p.Val643Ile) rs149425237
NM_000302.4(PLOD1):c.2050C>T (p.Arg684Cys) rs748841458
NM_000302.4(PLOD1):c.2068_2069delinsGT (p.Arg690Val) rs1553137685
NM_000302.4(PLOD1):c.2075C>T (p.Pro692Leu) rs557317492
NM_000302.4(PLOD1):c.2124T>C (p.His708=) rs879690
NM_000302.4(PLOD1):c.2133C>G (p.Leu711=) rs879691
NM_000302.4(PLOD1):c.214G>T (p.Ala72Ser) rs1343912990
NM_000302.4(PLOD1):c.2175C>T (p.Val725=) rs768818916
NM_000302.4(PLOD1):c.2181C>T (p.Pro727=) rs140741046
NM_000302.4(PLOD1):c.250G>A (p.Ala84Thr) rs34878020
NM_000302.4(PLOD1):c.265G>T (p.Ala89Ser) rs886039207
NM_000302.4(PLOD1):c.294C>T (p.Phe98=) rs7529452
NM_000302.4(PLOD1):c.295G>A (p.Ala99Thr) rs7551175
NM_000302.4(PLOD1):c.303C>T (p.Ser101=) rs147980436
NM_000302.4(PLOD1):c.307G>A (p.Asp103Asn) rs774590964
NM_000302.4(PLOD1):c.30G>C (p.Leu10=) rs886039113
NM_000302.4(PLOD1):c.323C>T (p.Ser108Leu) rs549517196
NM_000302.4(PLOD1):c.336G>A (p.Glu112=) rs746999816
NM_000302.4(PLOD1):c.353G>A (p.Arg118Gln) rs781455578
NM_000302.4(PLOD1):c.354G>C (p.Arg118=) rs746072884
NM_000302.4(PLOD1):c.358G>T (p.Ala120Ser) rs2273285
NM_000302.4(PLOD1):c.404_423del (p.Asp135fs) rs745409628
NM_000302.4(PLOD1):c.509A>T (p.Glu170Val) rs554232128
NM_000302.4(PLOD1):c.52G>A (p.Ala18Thr) rs373165011
NM_000302.4(PLOD1):c.534C>T (p.Ser178=) rs113384442
NM_000302.4(PLOD1):c.535G>T (p.Asp179Tyr) rs188165334
NM_000302.4(PLOD1):c.540G>A (p.Gln180=) rs35958757
NM_000302.4(PLOD1):c.555G>T (p.Lys185Asn) rs142978362
NM_000302.4(PLOD1):c.564G>C (p.Leu188Phe) rs201888323
NM_000302.4(PLOD1):c.579G>T (p.Arg193Ser) rs1553134266
NM_000302.4(PLOD1):c.652G>A (p.Val218Met) rs372534520
NM_000302.4(PLOD1):c.656T>C (p.Leu219Pro) rs1392799816
NM_000302.4(PLOD1):c.741+4G>C rs763641520
NM_000302.4(PLOD1):c.776G>A (p.Arg259His) rs144226170
NM_000302.4(PLOD1):c.802A>G (p.Thr268Ala) rs74354225
NM_000302.4(PLOD1):c.804C>T (p.Thr268=) rs140758113
NM_000302.4(PLOD1):c.805G>A (p.Val269Met) rs145447578
NM_000302.4(PLOD1):c.842G>A (p.Gly281Glu) rs1056398577
NM_000302.4(PLOD1):c.870C>T (p.Val290=) rs373082170
NM_000302.4(PLOD1):c.897G>A (p.Pro299=) rs199946373
NM_000302.4(PLOD1):c.936C>T (p.His312=) rs374787907
NM_000302.4(PLOD1):c.95C>T (p.Thr32Met) rs374597380
NM_000302.4(PLOD1):c.975C>T (p.His325=) rs761576315

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