ClinVar (all) for Orgtrack (Select 505807) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 226450	NM_000237.3(LPL):c.1187A>T (p.Glu396Val)	LPL (E396V)	Single nucleotide variant (missense variant)	Hyperlipoproteinemia, type I	GLikely pathogenic
Select item 226449	NM_000237.3(LPL):c.928T>C (p.Cys310Arg)	LPL (C310R)	Single nucleotide variant (missense variant)	Hyperlipoproteinemia, type I	GLikely pathogenic