ClinVar Miner

List of variants in gene PLOD1 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_000302.3(PLOD1):c.-27C>A rs1252431057
NM_000302.3(PLOD1):c.-28delT rs1204442973
NM_000302.3(PLOD1):c.1098-3C>T rs541901674
NM_000302.3(PLOD1):c.1098-4G>A rs1553135998
NM_000302.3(PLOD1):c.1128C>T (p.Thr376=) rs1553136011
NM_000302.3(PLOD1):c.1149T>C (p.Ala383=) rs1051856481
NM_000302.3(PLOD1):c.1164C>T (p.Thr388=) rs74949176
NM_000302.3(PLOD1):c.1202+3G>A rs370358836
NM_000302.3(PLOD1):c.1203-3C>T rs376288573
NM_000302.3(PLOD1):c.1218G>A (p.Pro406=) rs754812888
NM_000302.3(PLOD1):c.1428G>A (p.Lys476=) rs139869965
NM_000302.3(PLOD1):c.1461C>T (p.Ile487=) rs746099980
NM_000302.3(PLOD1):c.1471-18C>T rs368968576
NM_000302.3(PLOD1):c.1471-9_1471-8delCCinsGT rs1553136318
NM_000302.3(PLOD1):c.1534C>T (p.Arg512Cys) rs138490756
NM_000302.3(PLOD1):c.1707G>A (p.Leu569=) rs139468110
NM_000302.3(PLOD1):c.1756-13C>T rs370882934
NM_000302.3(PLOD1):c.1818C>A (p.Ile606=) rs372579008
NM_000302.3(PLOD1):c.1902+13G>A rs199765551
NM_000302.3(PLOD1):c.1903-18C>T rs750758605
NM_000302.3(PLOD1):c.1927G>A (p.Val643Ile) rs149425237
NM_000302.3(PLOD1):c.2028+11G>C rs1057523876
NM_000302.3(PLOD1):c.276G>A (p.Glu92=) rs768169776
NM_000302.3(PLOD1):c.302+15G>A rs140227667
NM_000302.3(PLOD1):c.303C>T (p.Ser101=) rs147980436
NM_000302.3(PLOD1):c.509A>T (p.Glu170Val) rs554232128
NM_000302.3(PLOD1):c.555G>T (p.Lys185Asn) rs142978362
NM_000302.3(PLOD1):c.579+17G>A rs181015965
NM_000302.3(PLOD1):c.643+15C>T rs376661744
NM_000302.3(PLOD1):c.741+4G>A rs763641520
NM_000302.3(PLOD1):c.741+7G>A rs751215041
NM_000302.3(PLOD1):c.76+17C>T rs113691754
NM_000302.3(PLOD1):c.804C>T (p.Thr268=) rs140758113
NM_000302.3(PLOD1):c.843+17G>C rs201244598
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.975+13C>T rs79345327
NM_000302.3(PLOD1):c.976-16C>T rs142329815

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