List of variants in gene KCNE1 reported as benign for long QT 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: 32

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HGVS	dbSNP	gnomAD frequency
NM_000219.6(KCNE1):c.*2529C>T	rs2834485	0.69189
NM_000219.6(KCNE1):c.*1219A>G	rs11909074	0.50320
NM_000219.6(KCNE1):c.*2480A>G	rs3453	0.48112
NM_000219.6(KCNE1):c.*456C>T	rs2070356	0.48073
NM_000219.6(KCNE1):c.*124A>G	rs2070357	0.44827
NM_000219.5(KCNE1):c.-577C>T	rs11702354	0.23004
NM_000219.6(KCNE1):c.-252G>A	rs2834502	0.19962
NM_000219.6(KCNE1):c.*490G>C	rs41314067	0.16321
NM_000219.6(KCNE1):c.*132A>G	rs41314071	0.15224
NM_000219.6(KCNE1):c.*578T>C	rs16991703	0.14679
NM_000219.6(KCNE1):c.*1322A>G	rs11700621	0.13749
NM_000219.6(KCNE1):c.*2461A>G	rs13050198	0.06850
NM_000219.6(KCNE1):c.*1068A>C	rs41314803	0.03124
NM_000219.6(KCNE1):c.-253A>G	rs41315471	0.02496
NM_000219.6(KCNE1):c.*2103C>T	rs41312367	0.01957
NM_000219.6(KCNE1):c.*2098T>C	rs41312993	0.01820
NM_000219.6(KCNE1):c.-375A>G	rs41315349	0.01784
NM_000219.6(KCNE1):c.-50-288A>G	rs2070358	0.01366
NM_000219.6(KCNE1):c.*268C>T	rs41314807	0.01093
NM_000219.6(KCNE1):c.-464G>A	rs4817670	0.00871
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.-100T>C	rs41314819	0.00267
NM_000219.6(KCNE1):c.-198C>T	rs376688699	0.00019
NM_000219.6(KCNE1):c.112A>G (p.Ser38Gly)	rs1805127	0.00019
NM_000219.6(KCNE1):c.162C>T (p.Phe54=)	rs17173508	0.00012
NM_000219.6(KCNE1):c.139G>A (p.Val47Ile)	rs199473353	0.00005
NM_000219.6(KCNE1):c.30G>A (p.Thr10=)	rs187686559	0.00005
NM_000219.6(KCNE1):c.*1547dup	rs11373310
NM_000219.6(KCNE1):c.*1815A>G	rs57555550
NM_000219.6(KCNE1):c.*2007=	rs2211696
NM_000219.6(KCNE1):c.*2123G>A	rs41314793

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