"PreventionGenetics, part of Exact Sciences"[submitter] AND "LIPC"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 782593	NM_000236.3(LIPC):c.213G>A (p.Thr71=)	LIPC	Single nucleotide variant (synonymous variant)	Hyperlipidemia due to hepatic triglyceride lipase deficiency +2 more	GBenign/Likely benign
Select item 3049407	NM_000236.3(LIPC):c.693C>T (p.Ser231=)	LIPC	Single nucleotide variant (synonymous variant)	LIPC-related disorder	GLikely benign
Select item 316670	NM_000236.3(LIPC):c.1052-13TC[6]	LIPC	Microsatellite (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 316672	NM_000236.3(LIPC):c.1064A>G (p.Gln355Arg)	LIPC (Q355R)	Single nucleotide variant (missense variant)	High density lipoprotein cholesterol level quantitative trait locus 12 +4 more	GBenign/Likely benign
Select item 316676	NM_000236.3(LIPC):c.1203C>T (p.Ser401=)	LIPC	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 735412	NM_000236.3(LIPC):c.1226A>C (p.Asp409Ala)	LIPC (D409A)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity

ClinVar