rs199473355

Orientation

minus

Stabilized

minus

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

Make rs199473355(C;C)

Make rs199473355(C;T)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34449477

Gene

KCNE1

is a	snp
is	mentioned by
dbSNP	rs199473355
dbSNP (classic)	rs199473355
ClinGen	rs199473355
ebi	rs199473355
HLI	rs199473355
Exac	rs199473355
Gnomad	rs199473355
Varsome	rs199473355
LitVar	rs199473355
Map	rs199473355
PheGenI	rs199473355
Biobank	rs199473355
1000 genomes	rs199473355
hgdp	rs199473355
ensembl	rs199473355
geneview	rs199473355
scholar	rs199473355
google	rs199473355
pharmgkb	rs199473355
gwascentral	rs199473355
openSNP	rs199473355
23andMe	rs199473355
SNPshot	rs199473355
SNPdbe	rs199473355
MSV3d	rs199473355
GWAS Ctlg	rs199473355

Max Magnitude

0

ClinVar
Risk	rs199473355(C;C) rs199473355(G;G)
Alt	rs199473355(C;C) rs199473355(G;G)
Reference	Rs199473355(T;T)
Significance	Untested
Disease	not specified Congenital long QT syndrome
Variation	info
Gene	KCNE1B KCNE1
CLNDBN	not specified Congenital long QT syndrome
Reversed	1
HGVS	NC_000021.8:g.35821775A>C; NC_000021.8:g.35821775A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000223891.1, RCV000119068.2,