ClinVar Miner

List of variants in gene PLOD1 reported as benign

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Gene type:
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Total variants: 44
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HGVS dbSNP
GRCh37/hg19 1p36.22(chr1:11990197-12000670)x1
NM_000302.4(PLOD1):c.*614G>T
NM_000302.4(PLOD1):c.*71C>G rs2230899
NM_000302.4(PLOD1):c.1097+220T>C rs59578134
NM_000302.4(PLOD1):c.1141G>A (p.Val381Met) rs2230896
NM_000302.4(PLOD1):c.1164C>T (p.Thr388=) rs74949176
NM_000302.4(PLOD1):c.1206C>T (p.Asn402=) rs1130529
NM_000302.4(PLOD1):c.1329-20G>A rs78527487
NM_000302.4(PLOD1):c.1329-94T>A rs7529028
NM_000302.4(PLOD1):c.1470+81T>C rs7529312
NM_000302.4(PLOD1):c.1495C>T (p.Arg499Trp) rs149124387
NM_000302.4(PLOD1):c.1534C>T (p.Arg512Cys) rs138490756
NM_000302.4(PLOD1):c.1632A>C (p.Ala544=) rs2230898
NM_000302.4(PLOD1):c.168+79C>T rs744754
NM_000302.4(PLOD1):c.169-53C>G rs114595968
NM_000302.4(PLOD1):c.169-96C>T rs58469200
NM_000302.4(PLOD1):c.1756-280G>A rs11121846
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.2028+8G>T rs181951731
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.250G>A (p.Ala84Thr) rs34878020
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.302+15G>A rs140227667
NM_000302.4(PLOD1):c.302+83G>A rs41278622
NM_000302.4(PLOD1):c.358G>T (p.Ala120Ser) rs2273285
NM_000302.4(PLOD1):c.467-271A>G rs2273286
NM_000302.4(PLOD1):c.509A>T (p.Glu170Val) rs554232128
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.577A>C (p.Arg193=) rs569590633
NM_000302.4(PLOD1):c.579+274G>A rs72641005
NM_000302.4(PLOD1):c.644-17T>G rs41307745
NM_000302.4(PLOD1):c.76+17C>T rs113691754
NM_000302.4(PLOD1):c.76+264A>G rs1208984
NM_000302.4(PLOD1):c.802A>G (p.Thr268Ala) rs74354225
NM_000302.4(PLOD1):c.844-283T>C rs2273289
NM_000302.4(PLOD1):c.975+13C>T rs79345327
NM_000302.4(PLOD1):c.976-16C>T rs142329815
NM_000302.4(PLOD1):c.976-262G>A rs57286355
NM_000302.4(PLOD1):c.976-291A>G rs2207751

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