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. Author manuscript; available in PMC: 2011 Apr 13.
Published in final edited form as: Cancer Causes Control. 2010 Aug 15;21(11):1857–1866. doi: 10.1007/s10552-010-9613-7

Table 2.

Birth year-adjusted associations between oxidative stress and inflammatory-mediated pathway polymorphisms and breast cancer risk in the US Radiologic Technologists Study

Gene Entrez SNP IDa Genotype Cases (%)(n = 859) Controls (%)(n = 1,083) ORb 95% CI p-value p-trendc
IFNG rs1861494 AA 429 (51) 548 (51) 1.0
AG 342 (40) 429 (40) 1.0 0.8 1.2 0.8
GG 74 (9) 89 (8) 1.1 0.8 1.5 0.7 0.7
IFNG rs2069705 TT 369 (45) 478 (45) 1.0
TC 352 (43) 468 (44) 1.0 0.8 1.2 0.8
CC 105 (13) 119 (11) 1.1 0.9 1.5 0.4 0.6
IL1B rs16944 CC 370 (45) 456 (42) 1.0
TC 352 (43) 494 (46) 0.9 0.7 1.1 0.2
TT 98 (12) 127 (12) 1.0 0.7 1.3 0.7 0.4
IL1B rs1143634 CC 463 (56) 636 (59) 1.0
TC 314 (38) 385 (36) 1.1 0.8 1.4 0.3
TT 57 (7) 53 (5) 1.5 1.0 2.2 0.05 0.05
IL4 rs2243250 CC 616 (74) 750 (70) 1.0
TC 206 (25) 289 (27) 0.9 0.7 1.1 0.2
TT 16 (2) 35 (3) 0.5 0.3 1.0 0.05 0.08
IL4d rs2243248 TT 721 (86) 928 (89) 1.0
GT/GG 115 (14) 120 (11) 1.2 0.9 1.6 0.1 0.2
IL4 rs2070874 CC 600 (73) 763 (71) 1.0
TC 206 (25) 288 (27) 0.9 0.7 1.1 0.4
TT 12 (1) 30 (3) 0.5 0.3 1.0 0.05 0.03
IL6e rs1800795 GG 274 (33) 379 (35) 1.0
CG 408 (49) 487 (45) 1.2 0.9 1.4 0.2
CC 156 (19) 211 (20) 1.0 0.8 1.3 0.9 0.6
IL6f rs1800797 GG 272 (33) 393 (37) 1.0
GA 395 (48) 478 (45) 1.2 1.0 1.5 0.09
AA 151 (18) 199 (19) 1.1 0.8 1.4 0.5 0.3
IL10 rs1800871 CC 487 (59) 590 (56) 1.0
TC 288 (35) 394 (37) 0.9 0.7 1.1 0.2
TT 54 (7) 75 (7) 0.9 0.6 1.3 0.5 0.2
IL10 rs1800896 AA 219 (26) 322 (30) 1.0
GA 417 (50) 530 (50) 1.2 0.9 1.4 0.2
GG 200 (24) 230 (21) 1.3 1.0 1.7 0.06 0.06
IL12B rs3212227 AA 537 (64) 697 (64) 1.0
CA 263 (31) 335 (31) 1.0 0.8 1.2 0.9
CC 36 (4) 50 (5) 0.9 0.6 1.5 0.8 0.9
NFKB1 rs230521 GG 321 (38) 401 (37) 1.0
CG 400 (47) 496 (46) 1.0 0.8 1.2 0.9
CC 127 (15) 179 (17) 0.9 0.7 1.2 0.4 0.5
NFKBIE rs730775 TT 291 (34) 351 (33) 1.0
CT 425 (50) 547 (51) 0.9 0.8 1.1 0.5
CC 140 (16) 182 (17) 0.9 0.7 1.2 0.6 0.5
NOS2A rs944722 AA 309 (37) 407 (38) 1.0
GA 400 (48) 490 (45) 1.1 0.9 1.3 0.5
GG 123 (15) 182 (17) 0.9 0.7 1.2 0.3 0.6
NOS2A rs2297518 CC 526 (63) 675 (63) 1.0
TC 281 (34) 352 (34) 1.0 0.8 1.2 0.8
TT 30 (4) 45 (4) 0.9 0.5 1.4 0.5 0.8
NOS3 rs1799983 GG 412 (50) 506 (47) 1.0
TG 329 (40) 449 (42) 0.9 0.7 1.1 0.3
TT 77 (9) 122 (11) 0.8 0.6 1.1 0.1 0.09
NOS3 rs1549758 CC 418 (50) 516 (48) 1.0
TC 345 (41) 447 (42) 1.0 0.8 1.2 0.6
TT 72 (9) 114 (11) 0.8 0.6 1.1 0.1 0.2
PTGS1 rs5788 CC 615 (76) 799 (74) 1.0
CA 181 (22) 260 (24) 0.9 0.7 1.1 0.3
AA 17 (2) 20 (2) 1.1 0.6 2.1 0.8 0.5
PTGS2 rs5277 GG 610 (73) 794 (74) 1.0
GC 198 (24) 264 (24) 1.0 0.8 1.2 0.8
CC 23 (3) 20 (2) 1.5 0.8 2.7 0.2 0.6
PTGS2 rs5275 TT 387 (47) 437 (40) 1.0
TC 348 (42) 501 (46) 0.8 0.6 0.9 0.01
CC 96 (12) 144 (13) 0.8 0.6 1.0 0.06 0.01
SOD1d rs2070424 AA 712 (85) 931 (86) 1.0
GA/GG 124 (15) 149 (14) 1.1 0.8 1.4 0.5 0.4
SOD2 rs4880 CC 206 (24) 285 (26) 1.0
CT 422 (50) 539 (50) 1.1 0.9 1.3 0.5
TT 217 (26) 256 (24) 1.2 0.9 1.5 0.2 0.2
SOD2 rs2758346 AA 210 (25) 289 (27) 1.0
GA 416 (50) 534 (49) 1.1 0.9 1.3 0.5
GG 210 (25) 256 (24) 1.1 0.9 1.5 0.3 0.3
SOD3 rs2855262 CC 325 (40) 431 (40) 1.0
TC 398 (49) 516 (48) 1.0 0.8 1.2 0.8
TT 81 (11) 128 (12) 0.9 0.7 1.3 0.7 0.9
TNF rs1800629 GG 560 (69) 714 (67) 1.0
GA 229 (28) 313 (29) 0.9 0.8 1.1 0.5
AA 28 (3) 36 (3) 1.0 0.6 1.6 0.9 0.6
TNFd rs361525 GG 763 (91) 986 (91) 1.0
GA/AA 79 (9) 96 (9) 1.1 0.8 1.5 0.7 0.9
TNFd rs1799724 CC 682 (82) 898 (84) 1.0
TC/TT 148 (18) 174 (16) 1.1 0.9 1.4 0.4 0.3

Bolded p-trend values indicate significance ≤ 0.05

a

Entrez SNP reference ID number (http://www.ncbi.nlm.nih/gov/entry/query.fcgi?db=snp)

b

Adjusted for year of birth

c

1 df test across genotypes

d

Dominant model assumed due to prevalence of rare homozygotes <2%

e

p-value for Hardy–Weinberg equilibrium = 0.04

f

p-value for Hardy–Weinberg equilibrium = 0.03