highly significantp = 0.0029
The results for the second variant under investigation (rs1470579) demonstrated that the CC genotype was more frequent in the patients' group (9.4%) than the control group (4.3%), with the statistical analysis displaying a highly significant difference ( p = 0.0029) between the frequencies of the C allele in the patients' group (25.3%) and control group (16.8%), as reported in Table 6 and Figure 5 .