rs397508085

Orientation

plus

Stabilized

plus

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

Make rs397508085(-;G)

Make rs397508085(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2588752

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs397508085
dbSNP (classic)	rs397508085
ClinGen	rs397508085
ebi	rs397508085
HLI	rs397508085
Exac	rs397508085
Gnomad	rs397508085
Varsome	rs397508085
LitVar	rs397508085
Map	rs397508085
PheGenI	rs397508085
Biobank	rs397508085
1000 genomes	rs397508085
hgdp	rs397508085
ensembl	rs397508085
geneview	rs397508085
scholar	rs397508085
google	rs397508085
pharmgkb	rs397508085
gwascentral	rs397508085
openSNP	rs397508085
23andMe	rs397508085
SNPshot	rs397508085
SNPdbe	rs397508085
MSV3d	rs397508085
GWAS Ctlg	rs397508085

Max Magnitude

0

ClinVar
Risk	rs397508085(G;G)
Alt	rs397508085(G;G)
Reference	Rs397508085(-;-)
Significance	Untested
Disease	Long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome, LQT1 subtype
Reversed	0
HGVS	NC_000011.9:g.2609982dupG
CLNSRC	ClinVar
CLNACC	RCV000045979.2,