Genome-wide association study identified CNP12587 region underlying height variation in Chinese females.

A raw p value <0.05 was considered nominally significant, which was further subjected to a Bonferroni correction to account for multiple testing in this study, where a significance level of 0.05/N (N = 198, i.e., the total number of the tested CNPs) was used as a significance threshold for a test ( p = 2.53×10 −4 ).

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