Skip to main content
. Author manuscript; available in PMC: 2015 Dec 1.
Published in final edited form as: Mutat Res. 2014 Dec 1;770:19–28. doi: 10.1016/j.mrfmmm.2014.08.009

Table 3.

Associations between TLR3 and TNFRSF1 and breast cancer risk, by ER/PR tumor phenotype.

Controls ER+/PR+ ER+/PR− ER−/PR+ ER−/PR− Multinomial P-values (raw; adjusted)2,3

N N OR1 (95% CI) N OR (95% CI) N OR (95% CI) N OR (95% CI)
TLR3 (rs5743305)4 0.011, 0.040
 TT 1321 528 1.00 101 1.00 10 1.00 157 1.00
 TA 1415 597 1.04 (0.91, 1.20) 106 0.97 (0.73, 1.29) 21 1.98 (0.93, 4.23) 201 1.20 (0.96, 1.50)
 AA 430 172 0.97 (0.79, 1.19) 28 0.82 (0.53, 1.27) 12 3.70 (1.58, 8.67) 57 1.11 (0.80, 1.53)
 P-value (raw; adjusted) 2 0.774, 1.000 0.387, 1.000 0.003,0.010 0.534, 1.000
TNFRSF1A (rs4149578)4 0.018, 0.053
 GG 2487 1000 1.00 184 1.00 33 1.00 350 1.00
 GA/AA 678 295 1.09 (0.93, 1.27) 50 0.99 (0.72, 1.38) 10 1.13 (0.55, 2.30) 64 0.67 (0.51, 0.89)
 P-value (raw; adjusted) 0.284, 0.851 0.971, 1.000 0.747, 1.000 0.006, 0.017
1

Odds Ratios (OR) and 95% Confidence Intervals (CI) adjusted for age, study, BMI during referent year, parity, and genetic ancestry.

2

P values for SNPs in table are unadjusted and adjusted for multiple comparisons using the step down Bonferroni correction.

3

Multinomial p values exclude controls.

4

ARTP p value for TLR3 for ER−/PR+ tumors was 0.011; ARTP p value for ER−/PR− tumors for TNFRSF1A was 0.023.