Table 2.
SNP | Chr | Position | Gene(s) | Role | Alleles | Frequency (MAF) | Call Rate (%) | p-HWE | OR (95% CI) | p value | |
---|---|---|---|---|---|---|---|---|---|---|---|
A/B | Cases | Controls | |||||||||
rs117601636 | 11 | 2,620,807 | KCNQ1 | ncRNA exonic | A/G | 0.085 | 0.093 | 100.00% | 0.79 | 0.90 (0.67–1.23) | 0.520 |
rs231362 | 11 | 2,670,241 | KCNQ1 | ncRNA exonic | C/T | 0.135 | 0.126 | 100.00% | 0.685 | 1.08 (0.84–1.40) | 0.546 |
rs231356 | 11 | 2,684,113 | KCNQ1 | ncRNA exonic | A/T | 0.216 | 0.224 | 99.90% | 0.307 | 0.96 (0.78–1.18) | 0.682 |
rs8181588 | 11 | 2,810,311 | KCNQ1 | Intronic | C/T | 0.349 | 0.39 | 99.80% | 0.851 | 0.84 (0.70–1.01) | 0.061 |
rs163177 | 11 | 2,817,183 | KCNQ1 | Intronic | C/T | 0.51 | 0.463 | 99.70% | 0.788 | 1.21 (1.01–1.44) | 0.036 * |
rs163184 | 11 | 2,825,839 | KCNQ1 | Intronic | G/T | 0.493 | 0.453 | 99.50% | 0.527 | 1.18 (0.99–1.40) | 0.071 |
rs2283228 | 11 | 2,828,300 | KCNQ1 | Intronic | A/C | 0.311 | 0.368 | 99.60% | 0.632 | 0.78 (0.65–0.93) | 0.007 * |
rs2237895 | 11 | 2,835,964 | KCNQ1 | Intronic | A/C | 0.381 | 0.338 | 99.60% | 0.319 | 1.20 (1.00–1.44) | 0.046 * |
Notes: p-HWE > 0.05 indicates that the genotypes were in Hardy-Weinberg Equilibrium; p values were calculated with Pearson’s χ 2 tests; *p values ≤ 0.05 indicates statistical significance. Data in bold are statistically significant (p < 0.05).
Abbreviations: SNP, single nucleotide polymorphism; Alleles A/B, Minor/Major alleles; MAF, minor allele frequency; OR, odds ratio; CI, confidence interval; HWE, Hardy–Weinberg equilibrium; Chr, chromosome; KCNQ1, Potassium Voltage-Gated Channel Subfamily Q Member 1.