TABLE 4.
Gene | SNP | Position | Dominant p-values | Additive p-values | Recessive p-values, (OR, 95% CI) |
ADH1B: Missense Variantc.143A > G, p.His48Arg | rs1229984 | chr4:99318162 | M: 0.46, F: 0.78 | M: 0.41, F: 1.00 | M: 0.58, F: 0.59 |
ADH1C: Synonymous Variant, c.453T > A,C p.Thr151 = | rs2241894 | chr4:99344976 | M: 0.24, F: 0.39 | M: 0.09, F: 0.29 | M: 0.08, F: 0.72 |
ALDH1B1: Missense Variant, c.320G > A, p.Arg107His | rs2073478 | chr9:38396068 | M: 0.12, F: 0.12 | M: 0.34, F: 0.40 | M: 0.72, F: 0.77 |
ALDH2: 2KB Upstream Variant, A > G | rs886205 | chr12:111766623 | M: 0.48 F: 0.51 | M: 0.19, F: 0.46 | M: NA, F: 0.60 |
ALDH2: Missense Variant, c.1510G > A, p.Glu504Lys | rs671 | chr12:111803962 | M: 0.57, F: 0.65 | M: 0.39, F: 0.56 | M: 0.29, F: 0.59 |
M, male, F, female, NA, not applicable, OR, odds ratio, 95% CI = 95% confidence interval, Logistic regression was performed, adjusting for age, education, HTN, DM, and alcohol use. p-value with Bonferroni correction for significance was 0.01.