List of variants in gene KCNE1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 37

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HGVS	dbSNP	gnomAD frequency
NM_000219.6(KCNE1):c.*2461A>G	rs13050198	0.06850
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.*268C>T	rs41314807	0.01093
NM_000219.6(KCNE1):c.253G>A (p.Asp85Asn)	rs1805128	0.00841
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.*493C>T	rs77190660	0.00371
NM_000219.6(KCNE1):c.-377+13G>A	rs41315351	0.00323
NM_000219.6(KCNE1):c.-100T>C	rs41314819	0.00267
NM_000219.6(KCNE1):c.*1338C>T	rs74508995	0.00201
NM_000219.6(KCNE1):c.*817A>G	rs75375964	0.00188
NM_000219.5(KCNE1):c.-628A>G	rs76210431	0.00186
NM_000219.6(KCNE1):c.*1838T>A	rs41312369	0.00083
NM_000219.6(KCNE1):c.*2001G>A	rs41314799	0.00083
NM_000219.6(KCNE1):c.*30C>G	rs150963475	0.00061
NM_000219.6(KCNE1):c.*196C>G	rs76568182	0.00054
NM_000219.6(KCNE1):c.-531C>T	rs41315473	0.00039
NM_000219.6(KCNE1):c.*1574C>T	rs561997378	0.00033
NM_000219.6(KCNE1):c.374C>T (p.Thr125Met)	rs142511345	0.00027
NM_000219.6(KCNE1):c.*373A>G	rs41314805	0.00022
NM_000219.6(KCNE1):c.*1666G>A	rs181999033	0.00019
NM_000219.6(KCNE1):c.111C>T (p.Ser37=)	rs150458884	0.00015
NM_000219.6(KCNE1):c.162C>T (p.Phe54=)	rs17173508	0.00012
NM_000219.6(KCNE1):c.-82T>G	rs145416040	0.00010
NM_000219.6(KCNE1):c.29C>T (p.Thr10Met)	rs144917638	0.00007
NM_000219.6(KCNE1):c.*2000C>T	rs544071641	0.00006
NM_000219.6(KCNE1):c.-432G>A	rs539503433	0.00005
NM_000219.6(KCNE1):c.30G>A (p.Thr10=)	rs187686559	0.00005
NM_000219.6(KCNE1):c.*2150G>A	rs530554373	0.00003
NM_000219.6(KCNE1):c.*2194T>C	rs529806670	0.00003
NM_000219.6(KCNE1):c.*1815A>G	rs57555550
NM_000219.6(KCNE1):c.*553A>G	rs570907779
NM_000219.6(KCNE1):c.*923G>A	rs182050647
NM_000219.6(KCNE1):c.*946del	rs142762112

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