rs7250581

plus

Geno	Mag	Summary
(A;A)		normal
(A;G)	0	normal
(G;G)	2	1.4x risk

Reference

GRCh38 38.1/141

Chromosome

19

Position

29573489

is a	snp
is	mentioned by
dbSNP	rs7250581
dbSNP (classic)	rs7250581
ClinGen	rs7250581
ebi	rs7250581
HLI	rs7250581
Exac	rs7250581
Gnomad	rs7250581
Varsome	rs7250581
LitVar	rs7250581
Map	rs7250581
PheGenI	rs7250581
Biobank	rs7250581
1000 genomes	rs7250581
hgdp	rs7250581
ensembl	rs7250581
geneview	rs7250581
scholar	rs7250581
google	rs7250581
pharmgkb	rs7250581
gwascentral	rs7250581
openSNP	rs7250581
23andMe	rs7250581
SNPshot	rs7250581
SNPdbe	rs7250581
MSV3d	rs7250581
GWAS Ctlg	rs7250581

GMAF

0.07668

Max Magnitude

2

?

(A;A) (A;G) (G;G)

28

rs7250581 has been reported in a large study to be associated with heart disease, in particular, coronary artery disease.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.06 (CI 0.79-1.43), and for homozygotes, 1.40 (CI 1.05-1.86). [PMID 17554300 ]

[PMID 19955471 ] Genetic Variants Identified in a European Genome-Wide Association Study That Were Found to Predict Incident Coronary Heart Disease in the Atherosclerosis Risk in Communities Study

[PMID 19956433 ] Genetics of coronary artery disease: focus on genome-wide association studies.