ClinVar Miner

List of variants in gene PLOD1 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 95
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HGVS dbSNP
NM_000302.4(PLOD1):c.*440G>C rs11553681
NM_000302.4(PLOD1):c.*71C>G rs2230899
NM_000302.4(PLOD1):c.-27C>A rs1252431057
NM_000302.4(PLOD1):c.-28del rs1204442973
NM_000302.4(PLOD1):c.1023C>T (p.Gly341=) rs755056846
NM_000302.4(PLOD1):c.1077A>G (p.Ala359=)
NM_000302.4(PLOD1):c.1083C>T (p.Ala361=) rs1159010003
NM_000302.4(PLOD1):c.1098-3C>T rs541901674
NM_000302.4(PLOD1):c.1098-4G>A rs1553135998
NM_000302.4(PLOD1):c.1098-89G>A
NM_000302.4(PLOD1):c.1110G>A (p.Arg370=) rs148644646
NM_000302.4(PLOD1):c.1128C>T (p.Thr376=) rs1553136011
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.1149T>C (p.Ala383=) rs1051856481
NM_000302.4(PLOD1):c.114C>T (p.Thr38=) rs11553679
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.1182G>C (p.Arg394=) rs144439284
NM_000302.4(PLOD1):c.1202+3G>A rs370358836
NM_000302.4(PLOD1):c.1203-3C>T rs376288573
NM_000302.4(PLOD1):c.1209C>T (p.Val403=) rs1401528073
NM_000302.4(PLOD1):c.1218G>A (p.Pro406=) rs754812888
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.1328+27T>G
NM_000302.4(PLOD1):c.135G>A (p.Lys45=) rs765354146
NM_000302.4(PLOD1):c.1428G>A (p.Lys476=) rs139869965
NM_000302.4(PLOD1):c.1461C>T (p.Ile487=) rs746099980
NM_000302.4(PLOD1):c.1470+14G>A rs761691961
NM_000302.4(PLOD1):c.1471-18C>T rs368968576
NM_000302.4(PLOD1):c.1471-9_1471-8delinsGT rs1553136318
NM_000302.4(PLOD1):c.1473T>C (p.Asp491=) rs139165192
NM_000302.4(PLOD1):c.1495C>T (p.Arg499Trp) rs149124387
NM_000302.4(PLOD1):c.1530C>T (p.Ser510=) rs1025133534
NM_000302.4(PLOD1):c.1534C>T (p.Arg512Cys) rs138490756
NM_000302.4(PLOD1):c.1581C>T (p.Pro527=) rs142934642
NM_000302.4(PLOD1):c.1582G>A (p.Glu528Lys) rs112250644
NM_000302.4(PLOD1):c.1608C>T (p.His536=) rs138289419
NM_000302.4(PLOD1):c.1632A>C (p.Ala544=) rs2230898
NM_000302.4(PLOD1):c.1651-10C>T rs755961387
NM_000302.4(PLOD1):c.1707G>A (p.Leu569=) rs139468110
NM_000302.4(PLOD1):c.1756-13C>T rs370882934
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.1818C>A (p.Ile606=) rs372579008
NM_000302.4(PLOD1):c.1818C>T (p.Ile606=) rs372579008
NM_000302.4(PLOD1):c.1902+13G>A rs199765551
NM_000302.4(PLOD1):c.1903-18C>T rs750758605
NM_000302.4(PLOD1):c.1927G>A (p.Val643Ile) rs149425237
NM_000302.4(PLOD1):c.2001C>T (p.Ala667=)
NM_000302.4(PLOD1):c.2028+11G>C rs1057523876
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.2175C>T (p.Val725=) rs768818916
NM_000302.4(PLOD1):c.2181C>T (p.Pro727=) rs140741046
NM_000302.4(PLOD1):c.243G>A (p.Leu81=) rs371574381
NM_000302.4(PLOD1):c.250G>A (p.Ala84Thr) rs34878020
NM_000302.4(PLOD1):c.276G>A (p.Glu92=) rs768169776
NM_000302.4(PLOD1):c.302+15G>A rs140227667
NM_000302.4(PLOD1):c.303-10C>T rs750987724
NM_000302.4(PLOD1):c.303C>T (p.Ser101=) rs147980436
NM_000302.4(PLOD1):c.30G>C (p.Leu10=) rs886039113
NM_000302.4(PLOD1):c.331C>A (p.Arg111=)
NM_000302.4(PLOD1):c.336G>A (p.Glu112=) rs746999816
NM_000302.4(PLOD1):c.354G>C (p.Arg118=) rs746072884
NM_000302.4(PLOD1):c.509A>T (p.Glu170Val) rs554232128
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.579+17G>A rs181015965
NM_000302.4(PLOD1):c.643+15C>T rs376661744
NM_000302.4(PLOD1):c.644-11C>T
NM_000302.4(PLOD1):c.678G>A (p.Val226=) rs371007185
NM_000302.4(PLOD1):c.741+4G>A rs763641520
NM_000302.4(PLOD1):c.741+7G>A rs751215041
NM_000302.4(PLOD1):c.76+17C>T rs113691754
NM_000302.4(PLOD1):c.77-7T>C rs371488160
NM_000302.4(PLOD1):c.774G>A (p.Pro258=) rs753994916
NM_000302.4(PLOD1):c.789C>T (p.Phe263=) rs908800499
NM_000302.4(PLOD1):c.804C>T (p.Thr268=) rs140758113
NM_000302.4(PLOD1):c.843+17G>C rs201244598
NM_000302.4(PLOD1):c.870C>T (p.Val290=) rs373082170
NM_000302.4(PLOD1):c.882C>T (p.Ile294=) rs747668784
NM_000302.4(PLOD1):c.897G>A (p.Pro299=) rs199946373
NM_000302.4(PLOD1):c.905C>A (p.Ser302Tyr) rs565765056
NM_000302.4(PLOD1):c.936C>T (p.His312=) rs374787907
NM_000302.4(PLOD1):c.951C>T (p.His317=) rs770032875
NM_000302.4(PLOD1):c.975+13C>T rs79345327
NM_000302.4(PLOD1):c.975C>T (p.His325=) rs761576315
NM_000302.4(PLOD1):c.976-16C>T rs142329815

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