rs13149020

Orientation

plus

Stabilized

plus

Make rs13149020(-;-)

Make rs13149020(-;A)

Make rs13149020(A;A)

Reference

GRCh38 38.1/141

Chromosome

4

Position

27192449

is a	snp
is	mentioned by
dbSNP	rs13149020
dbSNP (classic)	rs13149020
ClinGen	rs13149020
ebi	rs13149020
HLI	rs13149020
Exac	rs13149020
Gnomad	rs13149020
Varsome	rs13149020
LitVar	rs13149020
Map	rs13149020
PheGenI	rs13149020
Biobank	rs13149020
1000 genomes	rs13149020
hgdp	rs13149020
ensembl	rs13149020
geneview	rs13149020
scholar	rs13149020
google	rs13149020
pharmgkb	rs13149020
gwascentral	rs13149020
openSNP	rs13149020
23andMe	rs13149020
SNPshot	rs13149020
SNPdbe	rs13149020
MSV3d	rs13149020
GWAS Ctlg	rs13149020

GMAF

0.2227

Max Magnitude

0

GWAS snp
PMID	[PMID 23166209]
Trait	QT interval
Title	Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.
Risk Allele	A
P-val	8E-6
Odds Ratio	10.69 [6.06-15.32] unit increase

?	(A;C) (C;C)