List of variants in gene LPL 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000237.3(LPL):c.1428-80T>A	rs117910839	0.02070
NM_000237.3(LPL):c.1018+16T>C	rs59184895	0.01380
NM_000237.3(LPL):c.88+40G>A	rs141390463	0.01073
NM_000237.3(LPL):c.-283G>T	rs80351041	0.00790
NM_000237.3(LPL):c.430-125A>C	rs57345602	0.00650
NM_000237.3(LPL):c.430-6C>T	rs11570897	0.00461
NM_000237.3(LPL):c.775+138A>G	rs111255464	0.00405
NM_000237.3(LPL):c.542-130C>A	rs144254368	0.00347
NM_000237.3(LPL):c.429+20A>C	rs3735959	0.00233
NM_000237.3(LPL):c.786G>A (p.Gln262=)	rs140986245	0.00066
NM_000237.3(LPL):c.687T>C (p.His229=)	rs45607438	0.00022
NM_000237.3(LPL):c.-172_-171dup	rs146978295
NM_000237.3(LPL):c.250-256C>G	rs115589061

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