rs397508068

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;CTT)	5	Romano-Ward Long QT Syndrome
(CTT;CTT)	0	common in clinvar

Make rs397508068(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2583530

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs397508068
dbSNP (classic)	rs397508068
ClinGen	rs397508068
ebi	rs397508068
HLI	rs397508068
Exac	rs397508068
Gnomad	rs397508068
Varsome	rs397508068
LitVar	rs397508068
Map	rs397508068
PheGenI	rs397508068
Biobank	rs397508068
1000 genomes	rs397508068
hgdp	rs397508068
ensembl	rs397508068
geneview	rs397508068
scholar	rs397508068
google	rs397508068
pharmgkb	rs397508068
gwascentral	rs397508068
openSNP	rs397508068
23andMe	rs397508068
SNPshot	rs397508068
SNPdbe	rs397508068
MSV3d	rs397508068
GWAS Ctlg	rs397508068

Max Magnitude

5

ClinVar
Risk	rs397508068(-;-)
Alt	rs397508068(-;-)
Reference	Rs397508068(CTT;CTT)
Significance	Pathogenic
Disease	Long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2604760_2604762delCTT
CLNSRC
CLNACC	RCV000045930.3,