rs199473469

Orientation

plus

Stabilized

plus

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

Make rs199473469(A;G)

Make rs199473469(G;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2583444

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199473469
dbSNP (classic)	rs199473469
ClinGen	rs199473469
ebi	rs199473469
HLI	rs199473469
Exac	rs199473469
Gnomad	rs199473469
Varsome	rs199473469
LitVar	rs199473469
Map	rs199473469
PheGenI	rs199473469
Biobank	rs199473469
1000 genomes	rs199473469
hgdp	rs199473469
ensembl	rs199473469
geneview	rs199473469
scholar	rs199473469
google	rs199473469
pharmgkb	rs199473469
gwascentral	rs199473469
openSNP	rs199473469
23andMe	rs199473469
SNPshot	rs199473469
SNPdbe	rs199473469
MSV3d	rs199473469
GWAS Ctlg	rs199473469

Max Magnitude

0

ClinVar
Risk	rs199473469(G;G)
Alt	rs199473469(G;G)
Reference	Rs199473469(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2604674A>G
CLNSRC	ClinVar
CLNACC	RCV000057806.3,