Single locus results for tests that were significant (p<0.05) in the discovery sample set.

Significance was assessed using logistic regression, and odds ratios (OR) and confidence intervals (CI) shown are for minor allele carrier versus non-carrier. No variants were significantly associated in both the discovery and validation sample sets.本研究采用逻辑回归（logistic regression）进行显著性检验，文中展示的比值比（odds ratios, OR）与置信区间（confidence intervals, CI）均为次要等位基因携带者与非携带者的对比结果。在发现集与验证集样本中，均未发现存在显著关联的遗传变异。