List of variants in gene APOE reported as likely benign for Alzheimer disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000041.4(APOE):c.651C>T (p.Ala217=)	rs72654468	0.00090
NM_000041.4(APOE):c.69G>A (p.Ala23=)	rs111833428	0.00024
NM_000041.4(APOE):c.249C>T (p.Asp83=)	rs767980905	0.00003

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