List of variants in gene PLOD2 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_000935.2(PLOD2):c.-212C>T	rs564744346	0.01058
NM_182943.3(PLOD2):c.109+307C>T	rs114645517	0.00996
NM_182943.3(PLOD2):c.880-302A>C	rs141559084	0.00847
NM_182943.3(PLOD2):c.10T>A (p.Cys4Ser)	rs116803293	0.00701
NM_182943.3(PLOD2):c.1128-78_1128-77insT	rs536415937	0.00677
NM_182943.3(PLOD2):c.1128-145C>T	rs150167832	0.00586
NM_182943.3(PLOD2):c.1358+73A>G	rs114112088	0.00585
NM_182943.3(PLOD2):c.109+42C>T	rs145580714	0.00558
NM_182943.3(PLOD2):c.1743+224C>A	rs147506063	0.00538
NM_182943.3(PLOD2):c.1359-163A>G	rs144400529	0.00531
NM_182943.3(PLOD2):c.1128-79G>A	rs57931335	0.00493
NM_182943.3(PLOD2):c.*32T>C	rs148862685	0.00490
NM_182943.3(PLOD2):c.1677+206G>A	rs115390352	0.00458
NM_182943.3(PLOD2):c.-104G>T	rs573663835	0.00454
NM_182943.3(PLOD2):c.201+197T>C	rs185300274	0.00452
NM_182943.3(PLOD2):c.1232+124A>G	rs183548536	0.00427
NM_182943.3(PLOD2):c.616-146T>C	rs184053032	0.00398
NC_000003.12:g.146161760T>C	rs183977350	0.00367
NM_182943.3(PLOD2):c.679+171T>C	rs146584046	0.00319
NM_182943.3(PLOD2):c.2106G>C (p.Val702=)	rs147997412	0.00288
NM_182943.3(PLOD2):c.1644C>T (p.Asn548=)	rs150609339	0.00238
NM_182943.3(PLOD2):c.-4G>A	rs79161810	0.00173
NM_182943.3(PLOD2):c.1678-86G>A	rs145658936	0.00102
NM_182943.3(PLOD2):c.1108G>A (p.Glu370Lys)	rs147402171	0.00094
NM_182943.3(PLOD2):c.805G>A (p.Val269Ile)	rs147665692	0.00061
NM_182943.3(PLOD2):c.861C>T (p.Val287=)	rs573318217	0.00010
NM_182943.3(PLOD2):c.1943G>A (p.Arg648Gln)	rs748652746	0.00004
NM_182943.3(PLOD2):c.1005+88T>C	rs187728894
NM_182943.3(PLOD2):c.1232+83_1232+86del	rs60626732
NM_182943.3(PLOD2):c.1848+162del	rs202042741
NM_182943.3(PLOD2):c.2022A>T (p.Val674=)	rs763894955
NM_182943.3(PLOD2):c.339-181A>G	rs116303598

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