rs199472766

Orientation

plus

Stabilized

plus

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

Make rs199472766(C;C)

Make rs199472766(C;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2585296

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472766
dbSNP (classic)	rs199472766
ClinGen	rs199472766
ebi	rs199472766
HLI	rs199472766
Exac	rs199472766
Gnomad	rs199472766
Varsome	rs199472766
LitVar	rs199472766
Map	rs199472766
PheGenI	rs199472766
Biobank	rs199472766
1000 genomes	rs199472766
hgdp	rs199472766
ensembl	rs199472766
geneview	rs199472766
scholar	rs199472766
google	rs199472766
pharmgkb	rs199472766
gwascentral	rs199472766
openSNP	rs199472766
23andMe	rs199472766
SNPshot	rs199472766
SNPdbe	rs199472766
MSV3d	rs199472766
GWAS Ctlg	rs199472766

Max Magnitude

0

ClinVar
Risk	rs199472766(C;C)
Alt	rs199472766(C;C)
Reference	Rs199472766(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2606526T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057557.3,