Table 3.
Genome-wide association studies of myocardial infarction (MI) or coronary heart disease (CHD)
| Chromosomal locus | Gene symbol | Phenotype | SNP array | References |
|---|---|---|---|---|
| 6p21.3 | LTA | MI | Japanese SNP database | Ozaki et al. (2002) |
| 9p21.3 | CDKN2A/B (?) | CHD | 100 K custom array | McPherson et al. (2007) |
| 9p21.3 | CDKN2A/B (?) | MI | Hap 300 K array (Illumina) | Helgadottir et al. (2007) |
| 9p21.3 | CDKN2A/B (?) | CHD | GeneChip 500 K array (Affymetrix) | Wellcome Trust Case Control Consortium (2007) |
| 9p21.3 | CDKN2A/B (?) | CHD | GeneChip 500 K array (Affymetrix) | Samani et al. (2007) |