List of variants in gene APOE reported as uncertain significance for immune system disorder

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.805C>G (p.Arg269Gly)	rs267606661	0.00032
NM_000041.4(APOE):c.434G>A (p.Gly145Asp)	rs267606664	0.00013
NM_000041.4(APOE):c.688G>A (p.Glu230Lys)	rs567353589	0.00002

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