rs199473396

Orientation

plus

Stabilized

plus

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

Make rs199473396(A;G)

Make rs199473396(G;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2570698

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199473396
dbSNP (classic)	rs199473396
ClinGen	rs199473396
ebi	rs199473396
HLI	rs199473396
Exac	rs199473396
Gnomad	rs199473396
Varsome	rs199473396
LitVar	rs199473396
Map	rs199473396
PheGenI	rs199473396
Biobank	rs199473396
1000 genomes	rs199473396
hgdp	rs199473396
ensembl	rs199473396
geneview	rs199473396
scholar	rs199473396
google	rs199473396
pharmgkb	rs199473396
gwascentral	rs199473396
openSNP	rs199473396
23andMe	rs199473396
SNPshot	rs199473396
SNPdbe	rs199473396
MSV3d	rs199473396
GWAS Ctlg	rs199473396

Max Magnitude

0

ClinVar
Risk	rs199473396(G;G)
Alt	rs199473396(G;G)
Reference	Rs199473396(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.2591928A>G
CLNSRC	ClinVar
CLNACC	RCV000057696.3,