Table 3. Association of SLC5A2 variants with significant coronary artery disease.
| SNP | Genotype frequencies (controls/cases) | OR [95% CI] | P-value | ||
|---|---|---|---|---|---|
| AA | AB | BB | |||
| rs9934336 | 396/543 | 264/374 | 50/57 | 0.97 [0.83–1.14] | 0.701 |
| rs3813008 | 532/735 | 167/228 | 11/11 | 0.96 [0.78–1.18] | 0.680 |
| rs3116150 | 397/543 | 263/371 | 50/60 | 0.98 [0.84–1.15] | 0.814 |
Association between analyzed SLC5A2 variants and significant coronary stenosis determined by univariable logistic regression analysis under an additive model of inheritance.
Abbreviations: A, major allele, B, minor allele; CI, confidence interval; OR, odds ratio; SNP, single nucleotide polymorphism.