rs17589290

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs17589290(C;G)

Make rs17589290(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

112002081

is a	snp
is	mentioned by
dbSNP	rs17589290
dbSNP (classic)	rs17589290
ClinGen	rs17589290
ebi	rs17589290
HLI	rs17589290
Exac	rs17589290
Gnomad	rs17589290
Varsome	rs17589290
LitVar	rs17589290
Map	rs17589290
PheGenI	rs17589290
Biobank	rs17589290
1000 genomes	rs17589290
hgdp	rs17589290
ensembl	rs17589290
geneview	rs17589290
scholar	rs17589290
google	rs17589290
pharmgkb	rs17589290
gwascentral	rs17589290
openSNP	rs17589290
23andMe	rs17589290
SNPshot	rs17589290
SNPdbe	rs17589290
MSV3d	rs17589290
GWAS Ctlg	rs17589290

GMAF

0.05969

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

GWAS snp
PMID	[PMID 21347282]
Trait
Title	Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
Risk Allele
P-val	0.000006
Odds Ratio	1.4300 [1.22-1.67]