ClinVar for MedGen (Select 1381652) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 441269	NM_000041.3(APOE):c.[305C>G;388T>C]	APOE (C130R +3 more)	Single nucleotide variant (missense variant)	APOE5 VARIANT	Gassociation
Select item 441264	NM_000041.3(APOE):c.[487C>T;91G>A]	APOE (R163C +3 more)	Single nucleotide variant (missense variant)	Familial type 3 hyperlipoproteinemia	GPathogenic
Select item 440842	NM_000041.4(APOE):c.91G>A (p.Glu31Lys)	APOE (E31K +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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