"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "APOE"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 242765	NM_000041.4(APOE):c.137T>C (p.Leu46Pro)	APOE (L46P +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 2514464	NM_000041.4(APOE):c.192G>C (p.Gln64His)	APOE (Q90H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 17851	NM_000041.4(APOE):c.487C>T (p.Arg163Cys)	APOE (R163C +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 3380625	NM_000041.4(APOE):c.503G>A (p.Arg168His)	APOE (R168H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 17862	NM_000041.4(APOE):c.683G>A (p.Trp228Ter)	APOE (W228* +1 more)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
Select item 2572764	NM_000041.4(APOE):c.737G>C (p.Arg246Pro)	APOE (R246P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 478884	NM_000041.4(APOE):c.805C>G (p.Arg269Gly)	APOE (R269G +1 more)	Single nucleotide variant (missense variant)	Familial type 3 hyperlipoproteinemia +8 more	GUncertain significance

ClinVar