Table 4. Association of SLC5A2 variants with the incidence of future cardiovascular events.
| SNP | Genotype frequencies (controls/cases) | HR [95% CI] | P-value | ||
|---|---|---|---|---|---|
| AA | AB | BB | |||
| rs9934336 | 624/300 | 442/189 | 73/33 | 0.94 [0.82-1.09] | 0.410 |
| rs3813008 | 855/394 | 269/121 | 15/7 | 0.96 [0.80-1.15] | 0.650 |
| rs3116150 | 637/288 | 432/195 | 70/39 | 1.05 [0.92-1.21] | 0.478 |
Association between analyzed SLC5A2 variants and the incidence of future cardiovascular events was determined by univariable Cox regression analysis under an additive model of inheritance.
Abbreviations: A, major allele, B, minor allele; CI, confidence interval; HR, hazard ratio; SNP, single nucleotide polymorphism.