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rs7250581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) normal
(A;G) 0 normal
(G;G) 2 1.4x risk
ReferenceGRCh38 38.1/141
Chromosome19
Position29573489
is asnp
is mentioned by
dbSNPrs7250581
dbSNP (classic)rs7250581
ClinGenrs7250581
ebirs7250581
HLIrs7250581
Exacrs7250581
Gnomadrs7250581
Varsomers7250581
LitVarrs7250581
Maprs7250581
PheGenIrs7250581
Biobankrs7250581
1000 genomesrs7250581
hgdprs7250581
ensemblrs7250581
geneviewrs7250581
scholarrs7250581
googlers7250581
pharmgkbrs7250581
gwascentralrs7250581
openSNPrs7250581
23andMers7250581
SNPshotrs7250581
SNPdbers7250581
MSV3drs7250581
GWAS Ctlgrs7250581
GMAF0.07668
Max Magnitude2
? (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 17554300OA-icon.png]


[PMID 19955471OA-icon.png] 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 19956433OA-icon.png] Genetics of coronary artery disease: focus on genome-wide association studies.