rs199473409

Orientation

plus

Stabilized

plus

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

Make rs199473409(A;C)

Make rs199473409(C;C)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2585272

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199473409
dbSNP (classic)	rs199473409
ClinGen	rs199473409
ebi	rs199473409
HLI	rs199473409
Exac	rs199473409
Gnomad	rs199473409
Varsome	rs199473409
LitVar	rs199473409
Map	rs199473409
PheGenI	rs199473409
Biobank	rs199473409
1000 genomes	rs199473409
hgdp	rs199473409
ensembl	rs199473409
geneview	rs199473409
scholar	rs199473409
google	rs199473409
pharmgkb	rs199473409
gwascentral	rs199473409
openSNP	rs199473409
23andMe	rs199473409
SNPshot	rs199473409
SNPdbe	rs199473409
MSV3d	rs199473409
GWAS Ctlg	rs199473409

Max Magnitude

0

ClinVar
Risk	rs199473409(C;C)
Alt	rs199473409(C;C)
Reference	Rs199473409(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.2606502A>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057550.3,