rs1546498

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs1546498(C;T)

Make rs1546498(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

126697272

is a	snp
is	mentioned by
dbSNP	rs1546498
dbSNP (classic)	rs1546498
ClinGen	rs1546498
ebi	rs1546498
HLI	rs1546498
Exac	rs1546498
Gnomad	rs1546498
Varsome	rs1546498
LitVar	rs1546498
Map	rs1546498
PheGenI	rs1546498
Biobank	rs1546498
1000 genomes	rs1546498
hgdp	rs1546498
ensembl	rs1546498
geneview	rs1546498
scholar	rs1546498
google	rs1546498
pharmgkb	rs1546498
gwascentral	rs1546498
openSNP	rs1546498
23andMe	rs1546498
SNPshot	rs1546498
SNPdbe	rs1546498
MSV3d	rs1546498
GWAS Ctlg	rs1546498

GMAF

0.01102

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 23166209]
Trait	QT interval
Title	Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.
Risk Allele	C
P-val	2E-6
Odds Ratio	7.69 [4.57-10.81] unit increase