rs267607197

Orientation

plus

Stabilized

plus

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

Make rs267607197(A;A)

Make rs267607197(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2587690

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs267607197
dbSNP (classic)	rs267607197
ClinGen	rs267607197
ebi	rs267607197
HLI	rs267607197
Exac	rs267607197
Gnomad	rs267607197
Varsome	rs267607197
LitVar	rs267607197
Map	rs267607197
PheGenI	rs267607197
Biobank	rs267607197
1000 genomes	rs267607197
hgdp	rs267607197
ensembl	rs267607197
geneview	rs267607197
scholar	rs267607197
google	rs267607197
pharmgkb	rs267607197
gwascentral	rs267607197
openSNP	rs267607197
23andMe	rs267607197
SNPshot	rs267607197
SNPdbe	rs267607197
MSV3d	rs267607197
GWAS Ctlg	rs267607197

Max Magnitude

0

ClinVar
Risk	rs267607197(A;A)
Alt	rs267607197(A;A)
Reference	Rs267607197(G;G)
Significance	Pathogenic
Disease	Long QT syndrome 1
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome 1
Reversed	0
HGVS	NC_000011.9:g.2608920G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003296.2,