List of variants in gene KCNE1 reported as not provided for Congenital 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_000219.6(KCNE1):c.374C>T (p.Thr125Met)	rs142511345	0.00027
NM_000219.6(KCNE1):c.200G>A (p.Arg67His)	rs79654911	0.00019
NM_000219.6(KCNE1):c.83C>T (p.Ser28Leu)	rs199473350	0.00019
NM_000219.6(KCNE1):c.23C>T (p.Ala8Val)	rs199473348	0.00011
NM_000219.6(KCNE1):c.29C>T (p.Thr10Met)	rs144917638	0.00007
NM_000219.6(KCNE1):c.226G>A (p.Asp76Asn)	rs74315445	0.00005
NM_000219.6(KCNE1):c.95G>A (p.Arg32His)	rs17857111	0.00005
NM_000219.6(KCNE1):c.107G>A (p.Arg36His)	rs199473351	0.00003
NM_000219.6(KCNE1):c.163G>A (p.Gly55Ser)	rs199473644	0.00003
NM_000219.6(KCNE1):c.172A>C (p.Thr58Pro)	rs147187721	0.00003
NM_000219.6(KCNE1):c.176T>C (p.Leu59Pro)	rs141813529	0.00003
NM_000219.6(KCNE1):c.247G>A (p.Glu83Lys)	rs199473360	0.00003
NM_000219.6(KCNE1):c.221C>T (p.Ser74Leu)	rs74315446	0.00001
NM_000219.6(KCNE1):c.242A>G (p.Tyr81Cys)	rs199473359	0.00001
NM_000219.6(KCNE1):c.139G>T (p.Val47Phe)	rs199473353
NM_000219.6(KCNE1):c.154G>A (p.Gly52Arg)	rs199473354
NM_000219.6(KCNE1):c.158T>C (p.Phe53Ser)	rs199473355
NM_000219.6(KCNE1):c.199C>T (p.Arg67Cys)	rs199473645
NM_000219.6(KCNE1):c.209A>T (p.Lys70Met)	rs199473646
NM_000219.6(KCNE1):c.20C>T (p.Thr7Ile)	rs28933384
NM_000219.6(KCNE1):c.210G>C (p.Lys70Asn)	rs199473356
NM_000219.6(KCNE1):c.259T>C (p.Trp87Arg)	rs199473361
NM_000219.6(KCNE1):c.292C>T (p.Arg98Trp)	rs199473362
NM_000219.6(KCNE1):c.379C>A (p.Pro127Thr)	rs199473647
NM_000219.6(KCNE1):c.59C>T (p.Thr20Ile)	rs199473349

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