List of variants in gene KCNE1 reported as likely benign for Jervell and Lange-Nielsen syndrome

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_000219.6(KCNE1):c.1226_1229del	rs551512090	0.00693
NM_000219.5(KCNE1):c.-628A>G	rs76210431	0.00186
NM_000219.6(KCNE1):c.*946del	rs142762112

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