C0743924[trait identifier] AND "Phenosystems SA"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 36672	NM_174936.4(PCSK9):c.658-7C>T	PCSK9	Single nucleotide variant (intron variant)	Hypercholesterolemia, familial, 1 +5 more	GBenign
Select item 265933	NM_174936.4(PCSK9):c.709C>T (p.Arg237Trp)	PCSK9 (R237W +5 more)	Single nucleotide variant (missense variant)	Familial hypercholesterolemia +6 more	GConflicting classifications of pathogenicity
Select item 265943	NM_174936.4(PCSK9):c.1355-56C>T	PCSK9	Single nucleotide variant (intron variant)	Hypercholesterolemia, familial, 1 +1 more	GBenign

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