Variants with conflicting interpretations "risk factor" and "other"

Submission 1 (risk factor) minimum review status:		Submission 1 (risk factor) method:
Submission 2 (other) minimum review status:		Submission 2 (other) method:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

HGVS	dbSNP	gnomAD frequency
NM_000041.4(APOE):c.388T>C (p.Cys130Arg)	rs429358	0.16059
NM_000041.2(APOE):c.526C>T (p.Arg176Cys)	rs7412	0.07986
NM_000219.6(KCNE1):c.253G>A (p.Asp85Asn)	rs1805128	0.00841

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