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Genotypic association of variants at 9p21.3 chromosomal region with CAD.
| SNP | Model | Genotype | Frequency | Unadjusted | ||
|---|---|---|---|---|---|---|
| CASES | CONTROLS | OR (CI 95%) | p value | |||
| *rs7865618 | Codominant | AA | 0.180 | 0.374 | Reference | 3.86e10 |
| AG | 0.640 | 0.432 | 3.08 (2.18–4.37) | |||
| GG | 0.180 | 0.194 | 1.93 (1.25–2.99) | |||
| log-Additive p value 2.07e4 | ||||||
*SNP significant for the allelic association after multiple corrections. Bold indicates the details of significant genotype.
