Table 2.
Comparisons of genotype and allele frequencies between the case and the control groups for the relationship between functional COX-2 gene polymorphisms and susceptibility to oral cancer.
| SNP gene model | +837 T > C (rs5275) | −765 G > C (rs20417) | 1195 G > A (rs689466) | ||||||
|---|---|---|---|---|---|---|---|---|---|
| RR | 95% CI | P | RR | 95% CI | P | RR | 95% CI | P | |
| M allele versus W allele (allele model) | 0.87 | 0.77–0.98 | 0.021 | 0.66 | 0.58–0.76 | <0.001 | 0.94 | 0.87–1.02 | 0.164 |
| WM + MM versus WW (dominant model) | 0.53 | 0.40–0.72 | <0.001 | 0.72 | 0.64–0.82 | <0.001 | 0.95 | 0.89–1.02 | 0.186 |
| MM versus WW (homozygous model) | 0.68 | 0.47–0.99 | 0.042 | 0.26 | 0.16–0.43 | <0.001 | 0.85 | 0.71–1.01 | 0.069 |
| MM versus WM (heterozygous model) | 1.01 | 0.92–1.11 | 0.806 | 1.11 | 1.03–1.18 | 0.004 | 1.01 | 0.93–1.10 | 0.734 |
| MM versus WW + WM (recessive model) | 0.72 | 0.49–1.06 | 0.093 | 0.32 | 0.19–0.54 | <0.001 | 0.91 | 0.73–1.12 | 0.363 |
RR: relative risk; 95% CI: 95% confidential intervals.