rs199472706

Orientation

plus

Stabilized

plus

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

Make rs199472706(C;T)

Make rs199472706(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2571391

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472706
dbSNP (classic)	rs199472706
ClinGen	rs199472706
ebi	rs199472706
HLI	rs199472706
Exac	rs199472706
Gnomad	rs199472706
Varsome	rs199472706
LitVar	rs199472706
Map	rs199472706
PheGenI	rs199472706
Biobank	rs199472706
1000 genomes	rs199472706
hgdp	rs199472706
ensembl	rs199472706
geneview	rs199472706
scholar	rs199472706
google	rs199472706
pharmgkb	rs199472706
gwascentral	rs199472706
openSNP	rs199472706
23andMe	rs199472706
SNPshot	rs199472706
SNPdbe	rs199472706
MSV3d	rs199472706
GWAS Ctlg	rs199472706

Max Magnitude

0

ClinVar
Risk	rs199472706(T;T)
Alt	rs199472706(T;T)
Reference	Rs199472706(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2592621C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057729.3,