rs199473356

Orientation

minus

Stabilized

minus

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

Make rs199473356(C;C)

Make rs199473356(C;G)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34449425

Gene

KCNE1

is a	snp
is	mentioned by
dbSNP	rs199473356
dbSNP (classic)	rs199473356
ClinGen	rs199473356
ebi	rs199473356
HLI	rs199473356
Exac	rs199473356
Gnomad	rs199473356
Varsome	rs199473356
LitVar	rs199473356
Map	rs199473356
PheGenI	rs199473356
Biobank	rs199473356
1000 genomes	rs199473356
hgdp	rs199473356
ensembl	rs199473356
geneview	rs199473356
scholar	rs199473356
google	rs199473356
pharmgkb	rs199473356
gwascentral	rs199473356
openSNP	rs199473356
23andMe	rs199473356
SNPshot	rs199473356
SNPdbe	rs199473356
MSV3d	rs199473356
GWAS Ctlg	rs199473356

Max Magnitude

0

ClinVar
Risk	rs199473356(C;C)
Alt	rs199473356(C;C)
Reference	Rs199473356(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNE1B KCNE1
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000021.8:g.35821723C>G
CLNSRC	ClinVar
CLNACC	RCV000119077.2,