rs397508098

Orientation

plus

Stabilized

plus

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

Make rs397508098(A;A)

Make rs397508098(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2776985

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs397508098
dbSNP (classic)	rs397508098
ClinGen	rs397508098
ebi	rs397508098
HLI	rs397508098
Exac	rs397508098
Gnomad	rs397508098
Varsome	rs397508098
LitVar	rs397508098
Map	rs397508098
PheGenI	rs397508098
Biobank	rs397508098
1000 genomes	rs397508098
hgdp	rs397508098
ensembl	rs397508098
geneview	rs397508098
scholar	rs397508098
google	rs397508098
pharmgkb	rs397508098
gwascentral	rs397508098
openSNP	rs397508098
23andMe	rs397508098
SNPshot	rs397508098
SNPdbe	rs397508098
MSV3d	rs397508098
GWAS Ctlg	rs397508098

Max Magnitude

0

ClinVar
Risk	rs397508098(A;A)
Alt	rs397508098(A;A)
Reference	Rs397508098(G;G)
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.2798215G>A
CLNSRC	ClinVar
CLNACC	RCV000046013.2,