Two SNPs rs183532 and rs235875 as well as a haplotype TTC in <i>MYOC</i> were nominally associated with PACG despite the significance was lost after Bonferroni correction.
Two SNPs rs183532 and rs235875 as well as a haplotype TTC in <i>MYOC</i> were nominally associated with PACG despite the significance was lost after Bonferroni correction.
A comparison of the distributions of the genotypes and alleles of rs12076134 and rs235875 showed no statistically significant differences between the PACG patients and the controls (p>0.05).
The frequencies of the AA genotype and A allele of rs235913 were increased in PACG patients compared with controls, but the difference was not significant (p=0.037, p=0.017, respectively).