"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC130001 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3030487	NM_003383.5(VLDLR):c.7A>C (p.Thr3Pro)	LOC130001468, VLDLR +1 more (T3P)	Single nucleotide variant (non-coding transcript variant +1 more)	VLDLR-related disorder	GUncertain significance
Select item 130710	NM_003383.5(VLDLR):c.24G>A (p.Ala8=)	LOC130001468, VLDLR +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +4 more	GBenign/Likely benign