<b>Association Study Reveals a Susceptibility Locus with Male Pattern Baldness in the Han Chinese Population</b>

A total of 499 cases and 1489 controls were enrolled in this study. AGA represent "case", UC represent "control". SNPs were genotyped using the Sequenom MassArray platform (Sequenom Inc., San Diego, California, USA). The exclusion criteria for the genotyped SNPs were a call rate of less than 95% and a deviation from Hardy–Weinberg equilibrium (HWE, P &lt; 0.05) in the controls. Twenty-five SNPs passed the quality control and were subjected to statistical analysis. The Cochran–Armitage trend test was performed to evaluate the association between SNPs and MPB susceptibility. Two-tailed tests were conducted to calculate p-values. All statistical analyses were conducted using PLINK 1.07.<b>File: AGA_ALL.bed</b><b>Description:</b> Primary representation of genotype calls at biallelic variants.<b>File: AGA_ALL.bim</b><b>Description:</b> Extended variant information file accompanying a .bed binary genotype table.<b>File: AGA_ALL.fam</b><b>Description:</b> Samples information file accompanying a .bed binary genotype