rs199472688

Orientation

plus

Stabilized

plus

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

Make rs199472688(A;A)

Make rs199472688(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2527977

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472688
dbSNP (classic)	rs199472688
ClinGen	rs199472688
ebi	rs199472688
HLI	rs199472688
Exac	rs199472688
Gnomad	rs199472688
Varsome	rs199472688
LitVar	rs199472688
Map	rs199472688
PheGenI	rs199472688
Biobank	rs199472688
1000 genomes	rs199472688
hgdp	rs199472688
ensembl	rs199472688
geneview	rs199472688
scholar	rs199472688
google	rs199472688
pharmgkb	rs199472688
gwascentral	rs199472688
openSNP	rs199472688
23andMe	rs199472688
SNPshot	rs199472688
SNPdbe	rs199472688
MSV3d	rs199472688
GWAS Ctlg	rs199472688

Max Magnitude

0

ClinVar
Risk	rs199472688(A;A)
Alt	rs199472688(A;A)
Reference	Rs199472688(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.2549207G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000046057.2, RCV000057676.3,