RTEL1 and coronary artery disorder: As is shown in Table 3, logistic regression analyses revealed that the rs6010620 polymorphism in the RTEL1 gene conferred a decreased risk of CHD in the codominant model (adjusted: OR = 0.52, 95% CI: 0.31–0.88, p = 0.007 for the “G/G” genotype) and the recessive model (adjusted: OR = 0.49, 95% CI: 0.30–0.80, p = 0.004 for the “G/G” genotype).