rs397508096

Orientation

plus

Stabilized

plus

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

Make rs397508096(C;G)

Make rs397508096(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2445251

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs397508096
dbSNP (classic)	rs397508096
ClinGen	rs397508096
ebi	rs397508096
HLI	rs397508096
Exac	rs397508096
Gnomad	rs397508096
Varsome	rs397508096
LitVar	rs397508096
Map	rs397508096
PheGenI	rs397508096
Biobank	rs397508096
1000 genomes	rs397508096
hgdp	rs397508096
ensembl	rs397508096
geneview	rs397508096
scholar	rs397508096
google	rs397508096
pharmgkb	rs397508096
gwascentral	rs397508096
openSNP	rs397508096
23andMe	rs397508096
SNPshot	rs397508096
SNPdbe	rs397508096
MSV3d	rs397508096
GWAS Ctlg	rs397508096

Max Magnitude

0

ClinVar
Risk	rs397508096(G;G)
Alt	rs397508096(G;G)
Reference	Rs397508096(C;C)
Significance	Pathogenic
Disease	Long QT syndrome not provided
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.2466481C>G
CLNSRC	ClinVar
CLNACC	RCV000045993.3, RCV000182246.4,