Skip to main content
. 2017 Aug 14;8(51):88622–88629. doi: 10.18632/oncotarget.20242

Table 2. Genotype frequencies of TLR5 polymorphisms and their associations with breast cancer risk.

SNP Minor Major Case2 (%) Control3 (%) p4 for model of inheritance OR5 (95%CI)
(a1) (A) AA Aa aa AA Aa aa Additive Dominant Recessive
rs2072493 G A 292 176 48 270 197 53 0.321 0.132 0.629 0.828(0.649-1.058)
(56.6) (34.1) (9.3) (51.9) (37.9) (10.2)
rs5744168 T C 487 28 1 507 13 0 - 0.011 - 2.322(1.193-4.520)
(94.4) (5.4) (0.2) (97.1) (2.8) (0)

1Minor allele ‘a’ and the major ‘A’ are shown in the table. ‘AA’, ‘Aa’, ‘aa’ represent a given variant for each SNP genotyped.

2The number of cases in study cohort was 516.

3The number of controls in study cohort was 520.

4The p values were accessed using Plink and SPSS software under an additive model (AA vs. Aa vs. aa), dominant model (aa+Aa vs. AA), and recessive model (aa vs. Aa+AA) respectively. Significant values (P<0.05) are in bold.

5Estimated odds ratio (OR) and 95% confidence interval (CI) were assessed under a dominant model (aa+Aa vs. AA).