List of variants in gene KCNE1 reported as likely benign for not provided

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_000219.6(KCNE1):c.-162+68C>T	rs41313001	0.02084
NM_000219.6(KCNE1):c.*2098T>C	rs41312993	0.01820
NM_000219.6(KCNE1):c.*268C>T	rs41314807	0.01093
NM_000219.6(KCNE1):c.253G>A (p.Asp85Asn)	rs1805128	0.00841
NM_000219.6(KCNE1):c.-50-59T>C	rs2236608	0.00773
NM_000219.6(KCNE1):c.-50-60G>A	rs76165549	0.00745
NM_000219.6(KCNE1):c.1226_1229del	rs551512090	0.00693
NM_000219.6(KCNE1):c.84G>A (p.Ser28=)	rs17173510	0.00676
NM_000219.6(KCNE1):c.-162+24C>G	rs41312971	0.00564
NM_000219.6(KCNE1):c.-50-57C>T	rs74448880	0.00142
NM_000219.6(KCNE1):c.374C>T (p.Thr125Met)	rs142511345	0.00027
NM_000219.6(KCNE1):c.206A>G (p.Lys69Arg)	rs149338401	0.00024
NM_000219.6(KCNE1):c.162C>T (p.Phe54=)	rs17173508	0.00012
NM_000219.6(KCNE1):c.225C>T (p.Asn75=)	rs79175878	0.00009
NM_000219.6(KCNE1):c.252C>T (p.Ser84=)	rs138884514	0.00007
NM_000219.6(KCNE1):c.29C>T (p.Thr10Met)	rs144917638	0.00007
NM_000219.6(KCNE1):c.-162+12G>A	rs933665274	0.00006
NM_000219.6(KCNE1):c.-5C>A	rs191334763	0.00005
NM_000219.6(KCNE1):c.139G>A (p.Val47Ile)	rs199473353	0.00005
NM_000219.6(KCNE1):c.24G>A (p.Ala8=)	rs144094344	0.00005
NM_000219.6(KCNE1):c.222G>A (p.Ser74=)	rs766767618	0.00004
NM_000219.6(KCNE1):c.174C>G (p.Thr58=)	rs727503101	0.00002
NM_000219.6(KCNE1):c.*1815A>G	rs57555550
NM_000219.6(KCNE1):c.*2077GA[5]	rs41314795
NM_000219.6(KCNE1):c.*2123G>A	rs41314793
NM_000219.6(KCNE1):c.-161-91A>G	rs187207470
NM_000219.6(KCNE1):c.-50-128G>A	rs35811057
NM_000219.6(KCNE1):c.-50-156G>A	rs41314809
NM_000219.6(KCNE1):c.-51+3471del	rs11427854

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