rs199472691

Orientation

plus

Stabilized

plus

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

Make rs199472691(A;T)

Make rs199472691(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2570629

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472691
dbSNP (classic)	rs199472691
ClinGen	rs199472691
ebi	rs199472691
HLI	rs199472691
Exac	rs199472691
Gnomad	rs199472691
Varsome	rs199472691
LitVar	rs199472691
Map	rs199472691
PheGenI	rs199472691
Biobank	rs199472691
1000 genomes	rs199472691
hgdp	rs199472691
ensembl	rs199472691
geneview	rs199472691
scholar	rs199472691
google	rs199472691
pharmgkb	rs199472691
gwascentral	rs199472691
openSNP	rs199472691
23andMe	rs199472691
SNPshot	rs199472691
SNPdbe	rs199472691
MSV3d	rs199472691
GWAS Ctlg	rs199472691

Max Magnitude

0

ClinVar
Risk	rs199472691(T;T)
Alt	rs199472691(T;T)
Reference	Rs199472691(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2591859A>T
CLNSRC	ClinVar
CLNACC	RCV000057682.3,