| Rs1333042
|
| PubMed
|
[PMID 17478681 ]
|
| Affy Probeset
|
SNP_A-4215414
|
| Affy Orientation
|
same
|
| On GW 5.0
|
1
|
| Alleles A/B
|
A/G
|
| Ancestral
|
A
|
| Population
|
CEU
|
| Allele
|
G
|
| Case Freq.
|
|
| Control Freq.
|
|
| Odds Ratio Het
|
1.30
|
| Odds Ratio Hom
|
1.54
|
| Odds Ratio All
|
1.23
|
| Disease
|
Coronary artery disease (CAD)
|
rs1333042 increases susceptibility to Coronary artery disease 1.29 times for heterozygotes (AG) and 1.66 times for homozygotes (GG) [PMID 17478679]
rs1333042 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (AG) and 1.54 times for homozygotes (GG) [PMID 17478681]
rs1333042 increases susceptibility to Myocardial Infarction 1.36 times for heterozygotes (AG) and 1.84 times for homozygotes (GG) [PMID 17478679]
[PMID 20696043] Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort
[PMID 18987759] Genetic testing for atherosclerosis risk: inevitability or pipe dream?
[PMID 19214202] Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis.
[PMID 19578366] Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
[PMID 22882272] Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.
[PMID 32293292] Susceptible gene polymorphism in patients with three-vessel coronary artery disease.
]
