rs199472791

Orientation

plus

Stabilized

plus

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

Make rs199472791(C;T)

Make rs199472791(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2768903

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472791
dbSNP (classic)	rs199472791
ClinGen	rs199472791
ebi	rs199472791
HLI	rs199472791
Exac	rs199472791
Gnomad	rs199472791
Varsome	rs199472791
LitVar	rs199472791
Map	rs199472791
PheGenI	rs199472791
Biobank	rs199472791
1000 genomes	rs199472791
hgdp	rs199472791
ensembl	rs199472791
geneview	rs199472791
scholar	rs199472791
google	rs199472791
pharmgkb	rs199472791
gwascentral	rs199472791
openSNP	rs199472791
23andMe	rs199472791
SNPshot	rs199472791
SNPdbe	rs199472791
MSV3d	rs199472791
GWAS Ctlg	rs199472791

Max Magnitude

0

ClinVar
Risk	rs199472791(T;T)
Alt	rs199472791(T;T)
Reference	Rs199472791(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.2790133C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057601.3,