rs397508087

Orientation

plus

Stabilized

plus

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

Make rs397508087(-;-)

Make rs397508087(-;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2588804

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs397508087
dbSNP (classic)	rs397508087
ClinGen	rs397508087
ebi	rs397508087
HLI	rs397508087
Exac	rs397508087
Gnomad	rs397508087
Varsome	rs397508087
LitVar	rs397508087
Map	rs397508087
PheGenI	rs397508087
Biobank	rs397508087
1000 genomes	rs397508087
hgdp	rs397508087
ensembl	rs397508087
geneview	rs397508087
scholar	rs397508087
google	rs397508087
pharmgkb	rs397508087
gwascentral	rs397508087
openSNP	rs397508087
23andMe	rs397508087
SNPshot	rs397508087
SNPdbe	rs397508087
MSV3d	rs397508087
GWAS Ctlg	rs397508087

Max Magnitude

0

ClinVar
Risk	rs397508087(-;-)
Alt	rs397508087(-;-)
Reference	Rs397508087(C;C)
Significance	Pathogenic
Disease	Long QT syndrome Cardiac arrhythmia
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome, LQT1 subtype Cardiac arrhythmia
Reversed	0
HGVS	NC_000011.9:g.2610034delC
CLNSRC	ClinVar
CLNACC	RCV000045981.2, RCV000182281.1,