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. 2005 Oct 11;7(6):R987–R997. doi: 10.1186/bcr1333

Table 2.

Association between XRCC1 and XPD polymorphisms and breast cancer risk

Genotype Cases (%) Controls (%) OR (95% CI)a
XRCC1-280
Arg/Arg 399 (83.1) 406 (84.8) 1.0
Arg/His 78 (16.3) 70 (14.6)
His/His 3 (0.6) 3 (0.6) 1.15 (0.80–1.66)b
XRCC1-399
Arg/Arg 237 (49.5) 256 (53.6) 1.0
Arg/Gln 196 (40.9) 185 (38.7) 1.24 (0.93–1.65)
Gln/Gln 46 (9.6) 37 (7.7) 1.39 (0.84–2.29)c
Arg/Gln + Gln/Gln 242 (50.5) 222 (46.4) 1.26 (0.96–1.66)
XPD-751
Lys/Lys 147 (30.6) 155 (32.3) 1.0
Lys/Gln 238 (49.5) 237 (49.4) 1.03 (0.76–1.40)
Gln/Gln 96 (20.0) 88 (18.3) 1.10 (0.74–1.63)
Lys/Lys+Lys/Gln 385 (80.0) 325 (81.7) 1.0
Gln/Gln 96 (20.0) 88 (18.3) 1.08 (0.77–1.53)

aOdds ratios (ORs) and confidence intervals (CIs) adjusted for age, age at menarche, age at first full term pregnancy, number of pregnancies, history of benign breast disease, first degree family history of breast cancer, weist-to-hip ratio, smoking and use of alcohol. bOR for Arg/His and His/His genotypes combined. c p for trend = 0.105.