rs144917638

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs144917638(A;A)

Make rs144917638(A;G)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34449606

Gene

KCNE1

is a	snp
is	mentioned by
dbSNP	rs144917638
dbSNP (classic)	rs144917638
ClinGen	rs144917638
ebi	rs144917638
HLI	rs144917638
Exac	rs144917638
Gnomad	rs144917638
Varsome	rs144917638
LitVar	rs144917638
Map	rs144917638
PheGenI	rs144917638
Biobank	rs144917638
1000 genomes	rs144917638
hgdp	rs144917638
ensembl	rs144917638
geneview	rs144917638
scholar	rs144917638
google	rs144917638
pharmgkb	rs144917638
gwascentral	rs144917638
openSNP	rs144917638
23andMe	rs144917638
SNPshot	rs144917638
SNPdbe	rs144917638
MSV3d	rs144917638
GWAS Ctlg	rs144917638

Max Magnitude

0

ClinVar
Risk	rs144917638(A;A)
Alt	rs144917638(A;A)
Reference	Rs144917638(G;G)
Significance	Other
Disease	Congenital long QT syndrome Long QT syndrome not specified
Variation	info
Gene	KCNE1B KCNE1
CLNDBN	Congenital long QT syndrome Long QT syndrome not specified
Reversed	0
HGVS	NC_000021.8:g.35821904G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000119089.2, RCV000148515.2, RCV000208391.1,