Association of VDR genotype frequencies in PCa and control participants

SNPsGenotypes/
Alleles
Cancer cases N (%)Controls N (%)p-value (χ2)OR (95% CI)
rs1544410 BsmIBB16 (16%)30 (30%)0.9271 (Reference)
OR = 0.556; p = 0.446 (95% CI: 0.122–2.54)
OR = 0.952; p = 0.947 (95% CI: 0.226–4.01)
Bb38 (38%)28 (28%)
bb46 (46%)42 (42%)
B35%44%
b65%56%
rs7975232 ApaIAA42 (42%)41 (41%)0.045*1 (Reference)
OR = 1.67; p = 0.3 (95% CI: 0.632–4.39)
OR = 5.33; p = 0.024 (95% CI: 1.16–24.6)
Aa44 (44%)33 (33%)
aa14 (14%)26 (26%)
A64%57.5%
a36%42.5%
rs731236 TaqITT41 (41%)54 (54%)0.029*1 (Reference)
OR = 1.98; p = 0.037 (95% CI: 1.05–8.47)
OR = 4.63; p = 0.031 (95% CI: 1.09–19.7)
Tt45 (45%)27 (27%)
tt14 (14%)19 (19%)
T63.5%67.5%
t36.5%32.5%

SNPs: single nucleotide polymorphisms; OR: odds ratios; CI: confidence intervals; * statistically significant. Two OR are reported for each genotype. The first OR corresponds to the comparison between BB and Bb (AA and Aa) (TT and Tt) genotypes, and the second OR compares BB and bb (AA and aa) (TT and tt) genotypes. Each OR is accompanied by its p-value and 95% CI