ClinVar Miner

List of variants in gene PLOD1 reported as benign for Cardiovascular phenotype

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Total variants: 18
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HGVS dbSNP
NM_000302.3(PLOD1):c.1141G>A (p.Val381Met) rs2230896
NM_000302.3(PLOD1):c.1206C>T (p.Asn402=) rs1130529
NM_000302.3(PLOD1):c.1495C>T (p.Arg499Trp) rs149124387
NM_000302.3(PLOD1):c.1534C>T (p.Arg512Cys) rs138490756
NM_000302.3(PLOD1):c.1632A>C (p.Ala544=) rs2230898
NM_000302.3(PLOD1):c.177C>T (p.Gly59=) rs34032489
NM_000302.3(PLOD1):c.1788G>T (p.Val596=) rs35460537
NM_000302.3(PLOD1):c.2124T>C (p.His708=) rs879690
NM_000302.3(PLOD1):c.2133C>G (p.Leu711=) rs879691
NM_000302.3(PLOD1):c.250G>A (p.Ala84Thr) rs34878020
NM_000302.3(PLOD1):c.294C>T (p.Phe98=) rs7529452
NM_000302.3(PLOD1):c.295G>A (p.Ala99Thr) rs7551175
NM_000302.3(PLOD1):c.358G>T (p.Ala120Ser) rs2273285
NM_000302.3(PLOD1):c.509A>T (p.Glu170Val) rs554232128
NM_000302.3(PLOD1):c.540G>A (p.Gln180=) rs35958757
NM_000302.3(PLOD1):c.555G>T (p.Lys185Asn) rs142978362
NM_000302.3(PLOD1):c.564G>C (p.Leu188Phe) rs201888323
NM_000302.3(PLOD1):c.802A>G (p.Thr268Ala) rs74354225

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