List of variants in gene combination KCNE2, LOC105372791 reported as likely benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_172201.2(KCNE2):c.25C>G (p.Gln9Glu)	rs16991652	0.00468
NM_172201.2(KCNE2):c.22A>G (p.Thr8Ala)	rs2234916	0.00387
NM_172201.2(KCNE2):c.348G>A (p.Ala116=)	rs16991657	0.00002
NM_172201.2(KCNE2):c.318G>A (p.Ser106=)	rs781438592	0.00001

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