rs199473461

Orientation

plus

Stabilized

plus

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

Make rs199473461(C;C)

Make rs199473461(C;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2572894

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199473461
dbSNP (classic)	rs199473461
ClinGen	rs199473461
ebi	rs199473461
HLI	rs199473461
Exac	rs199473461
Gnomad	rs199473461
Varsome	rs199473461
LitVar	rs199473461
Map	rs199473461
PheGenI	rs199473461
Biobank	rs199473461
1000 genomes	rs199473461
hgdp	rs199473461
ensembl	rs199473461
geneview	rs199473461
scholar	rs199473461
google	rs199473461
pharmgkb	rs199473461
gwascentral	rs199473461
openSNP	rs199473461
23andMe	rs199473461
SNPshot	rs199473461
SNPdbe	rs199473461
MSV3d	rs199473461
GWAS Ctlg	rs199473461

Max Magnitude

0

ClinVar
Risk	rs199473461(C;C)
Alt	rs199473461(C;C)
Reference	Rs199473461(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.2594124T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057773.3,