"Clinical Genetics, Academic Medical Center"[submitter] AND "LPL"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1284647	NM_000237.3(LPL):c.286G>C (p.Val96Leu)	LPL (V96L)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 721152	NM_000237.3(LPL):c.456T>C (p.Asn152=)	LPL	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 1522	NM_000237.3(LPL):c.644G>A (p.Gly215Glu)	LPL (G215E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 1548	NM_000237.3(LPL):c.808C>T (p.Arg270Cys)	LPL (R270C)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GPathogenic
Select item 1530	NM_000237.3(LPL):c.809G>A (p.Arg270His)	LPL (R270H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 766071	NM_000237.3(LPL):c.1325T>G (p.Val442Gly)	LPL (V442G)	Single nucleotide variant (missense variant)	LPL-related disorder +5 more	GConflicting classifications of pathogenicity
Select item 1269038	NM_000237.3(LPL):c.1428-11C>T	LPL	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

ClinVar