rs199472679

Orientation

plus

Stabilized

plus

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

Make rs199472679(A;G)

Make rs199472679(G;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2445442

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472679
dbSNP (classic)	rs199472679
ClinGen	rs199472679
ebi	rs199472679
HLI	rs199472679
Exac	rs199472679
Gnomad	rs199472679
Varsome	rs199472679
LitVar	rs199472679
Map	rs199472679
PheGenI	rs199472679
Biobank	rs199472679
1000 genomes	rs199472679
hgdp	rs199472679
ensembl	rs199472679
geneview	rs199472679
scholar	rs199472679
google	rs199472679
pharmgkb	rs199472679
gwascentral	rs199472679
openSNP	rs199472679
23andMe	rs199472679
SNPshot	rs199472679
SNPdbe	rs199472679
MSV3d	rs199472679
GWAS Ctlg	rs199472679

Max Magnitude

0

ClinVar
Risk	rs199472679(G;G)
Alt	rs199472679(G;G)
Reference	Rs199472679(A;A)
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.2466672A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000046050.2, RCV000057661.3,