rs397508081

Orientation

plus

Stabilized

plus

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

Make rs397508081(-;-)

Make rs397508081(-;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2587630

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs397508081
dbSNP (classic)	rs397508081
ClinGen	rs397508081
ebi	rs397508081
HLI	rs397508081
Exac	rs397508081
Gnomad	rs397508081
Varsome	rs397508081
LitVar	rs397508081
Map	rs397508081
PheGenI	rs397508081
Biobank	rs397508081
1000 genomes	rs397508081
hgdp	rs397508081
ensembl	rs397508081
geneview	rs397508081
scholar	rs397508081
google	rs397508081
pharmgkb	rs397508081
gwascentral	rs397508081
openSNP	rs397508081
23andMe	rs397508081
SNPshot	rs397508081
SNPdbe	rs397508081
MSV3d	rs397508081
GWAS Ctlg	rs397508081

Max Magnitude

0

ClinVar
Risk	rs397508081(-;-)
Alt	rs397508081(-;-)
Reference	Rs397508081(C;C)
Significance	Untested
Disease	Jervell and Lange-Nielsen syndrome 1
Variation	info
Gene	KCNQ1
CLNDBN	Jervell and Lange-Nielsen syndrome 1
Reversed	0
HGVS	NC_000011.9:g.2608860delC
CLNSRC	ClinVar
CLNACC	RCV000045975.2,