"PreventionGenetics, part of Exact Sciences"[submitter] AND "APOE"[gen - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2635119	NM_000041.4(APOE):c.-24+47G>A	APOE (R7K)	Single nucleotide variant (missense variant +1 more)	APOE-related disorder	GUncertain significance
Select item 1722323	NM_000041.4(APOE):c.-24+82G>A	APOE (D19N)	Single nucleotide variant (missense variant +1 more)	Alzheimer disease 2 +1 more	GConflicting classifications of pathogenicity
Select item 3031963	NM_000041.4(APOE):c.165G>C (p.Leu55=)	APOE	Single nucleotide variant (synonymous variant)	APOE-related disorder +1 more	GLikely benign
Select item 2514464	NM_000041.4(APOE):c.192G>C (p.Gln64His)	APOE (Q90H +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 3047229	NM_000041.4(APOE):c.237-8G>C	APOE	Single nucleotide variant (intron variant)	APOE-related disorder	GLikely benign
Select item 3032874	NM_000041.4(APOE):c.387G>A (p.Val129=)	APOE	Single nucleotide variant (synonymous variant)	APOE-related disorder	GLikely benign
Select item 17851	NM_000041.4(APOE):c.487C>T (p.Arg163Cys)	APOE (R163C +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 3055012	NM_000041.4(APOE):c.495G>T (p.Arg165=)	APOE	Single nucleotide variant (synonymous variant)	APOE-related disorder	GLikely benign
Select item 1209955	NM_000041.4(APOE):c.786G>A (p.Glu262=)	APOE	Single nucleotide variant (synonymous variant)	APOE-related disorder +1 more	GLikely benign