List of variants in gene APOE reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000041.2(APOE):c.526C>T (p.Arg176Cys)	rs7412	0.07986
NM_000041.4(APOE):c.137T>C (p.Leu46Pro)	rs769452	0.00199
NM_000041.4(APOE):c.651C>T (p.Ala217=)	rs72654468	0.00090
NM_000041.4(APOE):c.120C>T (p.Ser40=)	rs373020952	0.00009
NM_000041.4(APOE):c.942C>T (p.Ser314=)	rs1051068315	0.00001
NM_000041.4(APOE):c.165G>C (p.Leu55=)

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