rs199473663

Orientation

plus

Stabilized

plus

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

Make rs199473663(G;T)

Make rs199473663(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2585280

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199473663
dbSNP (classic)	rs199473663
ClinGen	rs199473663
ebi	rs199473663
HLI	rs199473663
Exac	rs199473663
Gnomad	rs199473663
Varsome	rs199473663
LitVar	rs199473663
Map	rs199473663
PheGenI	rs199473663
Biobank	rs199473663
1000 genomes	rs199473663
hgdp	rs199473663
ensembl	rs199473663
geneview	rs199473663
scholar	rs199473663
google	rs199473663
pharmgkb	rs199473663
gwascentral	rs199473663
openSNP	rs199473663
23andMe	rs199473663
SNPshot	rs199473663
SNPdbe	rs199473663
MSV3d	rs199473663
GWAS Ctlg	rs199473663

Max Magnitude

0

ClinVar
Risk	rs199473663(T;T)
Alt	rs199473663(T;T)
Reference	Rs199473663(G;G)
Significance	Untested
Disease	Long QT syndrome Congenital long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome, LQT1 subtype Congenital long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2606510G>T
CLNSRC	ClinVar
CLNACC	RCV000045962.2, RCV000057554.3,