ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP gnomAD frequency
NM_000302.4(PLOD1):c.1098-89G>A rs72641011 0.02302
NM_000302.4(PLOD1):c.1097+326A>T rs148374791 0.01433
NM_000302.4(PLOD1):c.1650+79G>A rs115520586 0.01300
NM_000302.4(PLOD1):c.1097+219T>C rs112904654 0.00935
NM_000302.4(PLOD1):c.1098-230G>A rs147645440 0.00885
NM_000302.4(PLOD1):c.741+262A>G rs143846790 0.00864
NM_000302.4(PLOD1):c.2029-179C>T rs56868043 0.00760
NM_000302.4(PLOD1):c.302+15G>A rs140227667 0.00760
NM_000302.4(PLOD1):c.741+77G>A rs138253757 0.00753
NM_000302.4(PLOD1):c.76+93T>C rs111824694 0.00737
NM_000302.4(PLOD1):c.644-108A>T rs115737940 0.00723
NM_000302.4(PLOD1):c.1585-269C>T rs116001392 0.00683
NM_000302.4(PLOD1):c.1755+57G>A rs114809135 0.00680
NM_000302.4(PLOD1):c.77-216C>T rs79892860 0.00677
NM_000302.4(PLOD1):c.1755+106G>A rs116594838 0.00670
NM_000302.4(PLOD1):c.1903-335G>A rs116593479 0.00670
NM_000302.4(PLOD1):c.1756-75G>A rs6685691 0.00656
NM_000302.4(PLOD1):c.975+13C>T rs79345327 0.00627
NM_000302.4(PLOD1):c.843+220G>A rs116133545 0.00620
NM_000302.4(PLOD1):c.466+73G>A rs116340942 0.00601
NM_000302.4(PLOD1):c.1328+27T>G rs1338646628 0.00516
NM_000302.4(PLOD1):c.467-36G>A rs192592403 0.00508
NM_000302.4(PLOD1):c.1650+31C>A rs181227488 0.00503
NM_000302.4(PLOD1):c.76+17C>T rs113691754 0.00498
NM_000302.4(PLOD1):c.1203-237A>T rs115762130 0.00490
NM_000302.4(PLOD1):c.168+286C>T rs138210445 0.00479
NM_000302.4(PLOD1):c.1755+311G>T rs115100659 0.00477
NM_000302.4(PLOD1):c.303-115G>A rs77325770 0.00476
NM_000302.4(PLOD1):c.976-255C>T rs142176436 0.00409
NM_000302.4(PLOD1):c.1470+196G>A rs150192846 0.00371
NM_000302.4(PLOD1):c.644-194A>C rs147062976 0.00350
NM_000302.4(PLOD1):c.1534C>T (p.Arg512Cys) rs138490756 0.00328
NM_000302.4(PLOD1):c.1755+40G>A rs75453415 0.00317
NM_000302.4(PLOD1):c.467-245C>T rs114927523 0.00279
NM_000302.4(PLOD1):c.1902+13G>A rs199765551 0.00259
NM_000302.4(PLOD1):c.1164C>T (p.Thr388=) rs74949176 0.00170
NM_000302.4(PLOD1):c.1098-52C>A rs188970593 0.00169
NM_000302.4(PLOD1):c.1203-32C>T rs200325480 0.00160
NM_000302.4(PLOD1):c.843+17G>C rs201244598 0.00086
NM_000302.4(PLOD1):c.1582G>A (p.Glu528Lys) rs112250644 0.00077
NM_000302.4(PLOD1):c.776G>A (p.Arg259His) rs144226170 0.00076
NM_000302.4(PLOD1):c.976-16C>T rs142329815 0.00073
NM_000302.4(PLOD1):c.804C>T (p.Thr268=) rs140758113 0.00064
NM_000302.4(PLOD1):c.1927G>A (p.Val643Ile) rs149425237 0.00057
NM_000302.4(PLOD1):c.1473T>C (p.Asp491=) rs139165192 0.00052
NM_000302.4(PLOD1):c.579+17G>A rs181015965 0.00043
NM_000302.4(PLOD1):c.1756-13C>T rs370882934 0.00038
NM_000302.4(PLOD1):c.1707G>A (p.Leu569=) rs139468110 0.00034
NM_000302.4(PLOD1):c.1428G>A (p.Lys476=) rs139869965 0.00033
NM_000302.4(PLOD1):c.1495C>T (p.Arg499Trp) rs149124387 0.00030
NM_000302.4(PLOD1):c.1140C>T (p.Ser380=) rs200131516 0.00018
NM_000302.4(PLOD1):c.897G>A (p.Pro299=) rs199946373 0.00015
NM_000302.4(PLOD1):c.303C>T (p.Ser101=) rs147980436 0.00013
NM_000302.4(PLOD1):c.644-11C>T rs375303994 0.00013
NM_000302.4(PLOD1):c.1182G>C (p.Arg394=) rs144439284 0.00012
NM_000302.4(PLOD1):c.1203-3C>T rs376288573 0.00009
NM_000302.4(PLOD1):c.643+15C>T rs376661744 0.00008
NM_000302.4(PLOD1):c.1218G>A (p.Pro406=) rs754812888 0.00007
NM_000302.4(PLOD1):c.276G>A (p.Glu92=) rs768169776 0.00006
NM_000302.4(PLOD1):c.936C>T (p.His312=) rs374787907 0.00006
NM_000302.4(PLOD1):c.1202+3G>A rs370358836 0.00005
NM_000302.4(PLOD1):c.870C>T (p.Val290=) rs373082170 0.00005
NM_000302.4(PLOD1):c.1471-18C>T rs368968576 0.00004
NM_000302.4(PLOD1):c.243G>A (p.Leu81=) rs371574381 0.00004
NM_000302.4(PLOD1):c.-28del rs1204442973 0.00003
NM_000302.4(PLOD1):c.1098-3C>T rs541901674 0.00003
NM_000302.4(PLOD1):c.1818C>A (p.Ile606=) rs372579008 0.00003
NM_000302.4(PLOD1):c.*6C>T rs1254813319 0.00002
NM_000302.4(PLOD1):c.882C>T (p.Ile294=) rs747668784 0.00002
NM_000302.4(PLOD1):c.1149T>C (p.Ala383=) rs1051856481 0.00001
NM_000302.4(PLOD1):c.135G>A (p.Lys45=) rs765354146 0.00001
NM_000302.4(PLOD1):c.1461C>T (p.Ile487=) rs746099980 0.00001
NM_000302.4(PLOD1):c.309C>T (p.Asp103=) rs750096749 0.00001
NM_000302.4(PLOD1):c.466+3G>A rs779840832 0.00001
NM_000302.4(PLOD1):c.741+7G>A rs751215041 0.00001
NM_000302.4(PLOD1):c.-27C>A rs1252431057
NM_000302.4(PLOD1):c.1077A>G (p.Ala359=) rs1569713675
NM_000302.4(PLOD1):c.1098-4G>A rs1553135998
NM_000302.4(PLOD1):c.1128C>T (p.Thr376=) rs1553136011
NM_000302.4(PLOD1):c.1471-315del rs570781705
NM_000302.4(PLOD1):c.1471-80C>G rs180795740
NM_000302.4(PLOD1):c.1471-9_1471-8delinsGT rs1553136318
NM_000302.4(PLOD1):c.1584+138G>C rs78416567
NM_000302.4(PLOD1):c.1650+226del rs200184176
NM_000302.4(PLOD1):c.1903-128T>G rs116375338
NM_000302.4(PLOD1):c.1903-14dup rs748794198
NM_000302.4(PLOD1):c.1903-18C>T rs750758605
NM_000302.4(PLOD1):c.2001C>T (p.Ala667=) rs777554498
NM_000302.4(PLOD1):c.2028+11G>C rs1057523876
NM_000302.4(PLOD1):c.331C>A (p.Arg111=) rs772221158
NM_000302.4(PLOD1):c.467-35G>A rs183509111
NM_000302.4(PLOD1):c.467-35G>C rs183509111
NM_000302.4(PLOD1):c.741+4G>A rs763641520

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