ClinVar Miner

List of variants in gene PLOD1 reported as uncertain significance for Cardiovascular phenotype

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Total variants: 30
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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.1098-3C>T rs541901674
NM_000302.4(PLOD1):c.1145A>G (p.Asp382Gly) rs998178222
NM_000302.4(PLOD1):c.1172A>G (p.Asn391Ser) rs763409574
NM_000302.4(PLOD1):c.1203-3C>T rs376288573
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.1321C>T (p.Arg441Trp) rs11553676
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.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.214G>T (p.Ala72Ser) rs1343912990
NM_000302.4(PLOD1):c.265G>T (p.Ala89Ser) rs886039207
NM_000302.4(PLOD1):c.307G>A (p.Asp103Asn) rs774590964
NM_000302.4(PLOD1):c.323C>T (p.Ser108Leu) rs549517196
NM_000302.4(PLOD1):c.353G>A (p.Arg118Gln) rs781455578
NM_000302.4(PLOD1):c.52G>A (p.Ala18Thr) rs373165011
NM_000302.4(PLOD1):c.535G>T (p.Asp179Tyr) rs188165334
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.805G>A (p.Val269Met) rs145447578
NM_000302.4(PLOD1):c.842G>A (p.Gly281Glu) rs1056398577
NM_000302.4(PLOD1):c.95C>T (p.Thr32Met) rs374597380

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