Table 1 |
|||||
| Association test results for rs11571836 and CVD (SHARE + AP) | |||||
| Ethnicity | Individuals with at least one CVD event (% of total) | Individuals with no CVD events (n) | MAF (G allele)* | OR (95% CI) | P |
| All combined+ | 115 (10%) | 1063 | range: 0.15-.038 | 0.56 | 0.009 |
| Aboriginal | 55 (19%) | 235 | 0.15 | 0.42 (0.19-0.91) | 0.017 |
| South Asian | 32 (10%) | 291 | 0.23 | 0.43 (0.19-0.99) | 0.021 |
| European | 20 (8%) | 245 | 0.20 | 0.37 (0.08-1.63) | 0.19 |
| Chinese | 8 (3%) | 292 | 0.38 | 0.99 (0.35-2.9) | 0.99 |
+ meta-analysis (fixed-effect model) adjusted for multiple comparisons.
*MAF calculated from cases and controls combined for each ethnicity.
Zbuk et al. BMC Medical Genetics 2012 13:56 doi:10.1186/1471-2350-13-56
