ClinVar Miner

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

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Total variants: 23
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HGVS dbSNP
NM_000302.3(PLOD1):c.1083C>T (p.Ala361=) rs1159010003
NM_000302.3(PLOD1):c.1110G>A (p.Arg370=) rs148644646
NM_000302.3(PLOD1):c.1140C>T (p.Ser380=) rs200131516
NM_000302.3(PLOD1):c.1152C>T (p.Asp384=) rs771685198
NM_000302.3(PLOD1):c.1164C>T (p.Thr388=) rs74949176
NM_000302.3(PLOD1):c.1209C>T (p.Val403=) rs1401528073
NM_000302.3(PLOD1):c.1299C>T (p.Asp433=) rs886039111
NM_000302.3(PLOD1):c.1428G>A (p.Lys476=) rs139869965
NM_000302.3(PLOD1):c.1582G>A (p.Glu528Lys) rs112250644
NM_000302.3(PLOD1):c.1791G>C (p.Pro597=) rs151051718
NM_000302.3(PLOD1):c.2075C>T (p.Pro692Leu) rs557317492
NM_000302.3(PLOD1):c.2175C>T (p.Val725=) rs768818916
NM_000302.3(PLOD1):c.2181C>T (p.Pro727=) rs140741046
NM_000302.3(PLOD1):c.303C>T (p.Ser101=) rs147980436
NM_000302.3(PLOD1):c.30G>C (p.Leu10=) rs886039113
NM_000302.3(PLOD1):c.336G>A (p.Glu112=) rs746999816
NM_000302.3(PLOD1):c.354G>C (p.Arg118=) rs746072884
NM_000302.3(PLOD1):c.534C>T (p.Ser178=) rs113384442
NM_000302.3(PLOD1):c.804C>T (p.Thr268=) rs140758113
NM_000302.3(PLOD1):c.870C>T (p.Val290=) rs373082170
NM_000302.3(PLOD1):c.897G>A (p.Pro299=) rs199946373
NM_000302.3(PLOD1):c.936C>T (p.His312=) rs374787907
NM_000302.3(PLOD1):c.975C>T (p.His325=) rs761576315

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