C0020474[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333456	NM_000237.3(LPL):c.370T>C (p.Ser124Pro)	LPL (S124P)	Single nucleotide variant (missense variant)	Hyperlipidemia, familial combined, LPL related +1 more	GUncertain significance
Select item 855588	NM_000237.3(LPL):c.835C>G (p.Leu279Val)	LPL (L279V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GPathogenic