| Rs6475606
|
| PubMed
|
[PMID 17478681 ]
|
| Affy Probeset
|
SNP_A-4213421
|
| Affy Orientation
|
reverse
|
| On GW 5.0
|
1
|
| Alleles A/B
|
A/G
|
| Ancestral
|
T
|
| Population
|
CEU
|
| Allele
|
T
|
| Case Freq.
|
|
| Control Freq.
|
|
| Odds Ratio Het
|
1.30
|
| Odds Ratio Hom
|
1.54
|
| Odds Ratio All
|
1.23
|
| Disease
|
Coronary artery disease (CAD)
|
rs6475606 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (CT) and 1.54 times for homozygotes (TT) [PMID 17478681]
[PMID 18704761] Molecular genetics of myocardial infarction.
[PMID 18987759] Genetic testing for atherosclerosis risk: inevitability or pipe dream?
[PMID 19819472] Common genetic variants on chromosome 9p21 predict perioperative myocardial injury after coronary artery bypass graft surgery.
[PMID 21347282] Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.
[PMID 22961961] Genome-Wide Association Study of Intracranial Aneurysms Confirms Role of Anril and SOX17 in Disease Risk
[PMID 28057453] Association of ANRIL gene polymorphisms with major adverse cardiovascular events in hemodialysis patients.
[PMID 29228923] CDKN2BAS gene polymorphisms and the risk of intracranial aneurysm in the Chinese population.
[PMID 33285697] The association of CDKN2BAS gene polymorphisms and intracranial aneurysm: A meta-analysis.
]
