RS10757274 CDKN2B-AS1

Health Risk Chr 9:22096055 snv intron variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs10757274 is a SNP located in chromosomal region 9p21
Associated Conditions
GWAS Studies (14)
Trait Risk Allele OR / Beta P-value Study
Stable angina pectoris G OR: 0.16 2E-81 PubMed
Unstable angina pectoris G OR: 0.19 2E-52 PubMed
Coronary heart disease G OR: 1.37 8E-45 PubMed
Medication use (antithrombotic agents) G β: 0.067 1E-38 PubMed
Stable angina pectoris G OR: 0.15 5E-38 PubMed
Abdominal aortic aneurysm A OR: 1.24 2E-33 PubMed
Medication use (vasodilators used in cardiac diseases) G OR: 0.14 2E-33 PubMed
Medication use (salicylic acid and derivatives) G β: 0.099 1E-31 PubMed
Angina pectoris G OR: 0.15 2E-31 PubMed
Medication use (antithrombotic agents) G β: 0.085 4E-27 PubMed
Coronary artery disease G OR: 1.22 6E-27 PubMed
Unstable angina (intermediate coronary syndrome) (PheCode 411.1) 6E-16 PubMed
Ischemic heart disease (PheCode 411) 2E-13 PubMed
Coronary artery disease β: 0.075 8E-7 PubMed
Population Frequencies
1kG AFR
17.5%
1kG ALL
59.6%
1kG AMR
41.8%
1kG EAS
47.1%
1kG EUR
50.8%
1kG SAS
48.4%
Other Variants in CDKN2B-AS1
Ask Dr. Hemsworth about this variant