Association results (from 499 Graves' disease cases and 504 controls) of the four alleles with Bonferroni corrected P value smaller than 0.05.

aAll P values (except for those in the last column) reported were nominal P values. The study-wide significance cut-off nominal P value should be 0.00147 ( = 0.05/34, which is the Bonferroni correction for a total of 34 tested alleles). The statistically significance level for Bonferroni corrected P value (reported in the last column) should be 0.05. OR, odds ratio.

本次报告的所有P值（最后一列除外）均为名义P值（nominal P value）。全研究范围内的显著性临界名义P值应为0.00147（即0.05/34，为针对共计34个检测等位基因的邦弗朗尼（Bonferroni）校正值）。最后一列所报告的经邦弗朗尼校正的P值，其统计学显著性水准应为0.05。OR即比值比（odds ratio）。