Table 3. Allelic analysis of SNP rs3825214 association with AF and VT.
Cohort (cases/controls) | Frequency of G allele (cases/controls) | P-obs | P-adj | OR (95% CI) |
AF group | ||||
Male (424/543) | 0.419/0.455 | 0.117 | 0.091 | 0.81 (0.63–1.04) |
Female (259/310) | 0.407/0.450 | 0.148 | 0.143 | 0.76 (0.53–1.10) |
Total AF (692/856) | 0.414/0.452 | 0.036 | 0.025 | 0.79 (0.64–0.97) |
Lone AF (275/856) | 0.376/0.452 | 0.002 | 0.001 | 0.65 (0.50–0.84) |
Other AF (417/856) | 0.439/0.452 | 0.546 | 0.631 | 1.08 (0.80–1.45) |
CAD (175/856) | 0.446/0.452 | 0.927 | 0.361 | 0.80 (0.49–1.30) |
Hypertension (266/796) | 0.417/0.467 | 0.364 | 0.001 | 0.59 (0.43–0.81) |
T2DM (45/848) | 0.478/0.456 | 0.683 | 0.134 | 2.62 (0.74–9.27) |
Stroke (87/856) | 0.489/0.452 | 0.351 | 0.558 | 1.25 (0.60–2.62) |
VT group | ||||
Male (144/543) | 0.448/0.455 | 0.833 | 0.653 | 1.10 (0.73–1.66) |
Female (91/310) | 0.390/0.450 | 0.152 | 0.774 | 1.08 (0.64–1.83) |
Total VT (235/856) | 0.426/0.452 | 0.315 | 0.712 | 1.06 (0.77–1.47) |
AVB (24/856) | 0.292/0.452 | 0.028 | 0.035 | 0.49 (0.26–0.95) |
BBB (29/856) | 0.431/0.452 | 0.758 | 0.371 | 1.55 (0.59–4.03) |
Bradycardia (27/856) | 0.463/0.452 | 0.868 | 0.684 | 1.25 (0.42–3.71) |
ER (12/856) | 0.500/0.452 | 0.636 | 0.661 | 1.34 (0.37–4.89) |
HCM (26/856) | 0.365/0.452 | 0.219 | 0.674 | 1.20 (0.51–2.82) |
MVA (61/856) | 0.385/0.452 | 0.155 | 0.469 | 1.25 (0.69–2.27) |
BBB: bundle branch block; ER: early repolarization; HCM: hypertrophic cardiomyopathy; MVA: malignant ventricular arrhythmia.