Table 2. Summary of associations between 8 SNPs in ZFHX3 and the risk of AF.
SNP | Position | Minor/major allele | Casesa | Controlsa | MAF(cases) | MAF(controls) | P HWE | OR(95%CI) b | P b | P FDR c |
rs12596992 | 71536544 | C/G | 96/252/236 | 132/458/382 | 0.38 | 0.37 | 0.78 | 1.08(0.93–1.26) | 0.316 | 0.316 |
rs13336412 | 71539450 | A/C | 124/297/173 | 195/500/301 | 0.46 | 0.45 | 0.62 | 1.1(0.94–1.27) | 0.23 | 0.263 |
rs16971312 | 71413345 | G/A | 43/226/326 | 78/426/492 | 0.26 | 0.29 | 0.28 | 0.85(0.72–1.00) | 0.056 | 0.112 |
rs16971436 | 71550264 | G/T | 3/71/523 | 11/152/833 | 0.06 | 0.09 | 0.18 | 0.74(0.56–0.98) | 0.039 | 0.104 |
rs17680796 | 71538441 | T/C | 60/266/268 | 84/438/472 | 0.32 | 0.3 | 0.21 | 1.15(0.98–1.35) | 0.09 | 0.144 |
rs6499600 | 71536875 | T/C | 75/275/244 | 164/506/317 | 0.36 | 0.42 | 0.11 | 0.73(0.63–0.86) | 1.07×10−4 | 4.28×10−4 |
rs2106261 | 71609121 | A/G | 110/299/184 | 99/446/451 | 0.44 | 0.32 | 0.46 | 1.71(1.46–2.00) | 1.85×10−11 | 1.48×10−10 |
rs8049936 | 71642787 | G/A | 61/246/284 | 114/435/447 | 0.31 | 0.33 | 0.6 | 0.9(0.77–1.05) | 0.175 | 0.233 |
SNP, single nucleotide polymorphism; AF, atrial fibrillation; MAF, minor allele frequency; P HWE, P values for Hardy–Weinberg equilibrium tests in control groups; OR odds ratio; CI confidence interval.
Individuals homozygous for the minor allele/heterozygous/homozygous for the major allele.
OR (95%CI) and P values were derived from logistic regression analysis in the additive model adjusting for age, gender, hypertension, diabetes and coronary artery disease.
Multiple comparisons P values for false discovery rate.