Variants in gene KCNE1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_000219.6(KCNE1):c.253G>A (p.Asp85Asn)	rs1805128	0.00841
NM_000219.6(KCNE1):c.84G>A (p.Ser28=)	rs17173510	0.00676
NM_000219.6(KCNE1):c.162C>T (p.Phe54=)	rs17173508	0.00012
NM_000219.6(KCNE1):c.252C>T (p.Ser84=)	rs138884514	0.00007
NM_000219.6(KCNE1):c.-5C>A	rs191334763	0.00005
NM_000219.6(KCNE1):c.24G>A (p.Ala8=)	rs144094344	0.00005
NM_000219.6(KCNE1):c.30G>A (p.Thr10=)	rs187686559	0.00005
NM_000219.6(KCNE1):c.315G>A (p.Ser105=)	rs563859144	0.00005
NM_000219.6(KCNE1):c.174C>G (p.Thr58=)	rs727503101	0.00002

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