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. Author manuscript; available in PMC: 2015 Apr 1.
Published in final edited form as: Mutat Res. 2014 Mar 7;762:24–31. doi: 10.1016/j.mrfmmm.2014.02.004

Table 2.

Association between DNA repair genotypes and colon cancer risk by race

African Americans Whites

Cases/controls ORa 95% CI Cases/controls ORa 95%CI
XPD/ERCC2
DD 170 / 258 1.0 Ref 136 / 230 1.0 Ref
DN 45 / 60 1.1 (0.7, 1.8) 119 / 238 0.8 (0.6, 1.1)
NN 5 / 3 2.7 (0.6, 11.9) 40 / 57 1.2 (0.7, 1.8)
DN+NN 50 / 63 1.2 (0.8, 1.9) 159 / 295 0.9 (0.7, 1.2)
XPD/ERCC2
KK 128 / 186 1.0 Ref 114 / 209 1.0 Ref
KQ 83 / 115 1.1 (0.8, 1.6) 136 / 251 1.0 (0.7, 1.3)
QQ 13 / 19 1.0 (0.5, 2.1) 49 / 65 1.3 (0.9, 2.1)
KQ+QQ 96 / 134 1.1 (0.8, 1.5) 185 / 316 1.1 (0.8, 1.4)
XPF/ERCC4
RR 217 / 307 1.0 Ref 251 / 455 1.0 Ref
RQ 8 / 16 0.8 (0.3, 1.8) 52 / 74 1.3 (0.9, 1.9)
QQ 1 / 0 -- -- 1 / 7 0.3 (0.03, 2.1)
RQ+QQ 9 / 16 0.8 (0.4, 1.9) 53 / 81 1.2 (0.8, 1.7)
XPG/ERCC5
DD 65 / 100 1.0 Ref 183 / 335 1.0 Ref
DH 120 / 151 1.2 (0.8, 1.8) 100 / 170 1.1 (0.8, 1.5)
HH 39 / 66 0.9 (0.5, 1.5) 15 / 27 1.1 (0.5, 2.0)
DH+HH 159 / 217 1.1 (0.8, 1.6) 113 / 197 1.1 (0.8, 1.5)
XPC A499V
AA 175 / 276 1.0 Ref 177 / 293 1.0 Ref
AV 51 / 47 1.7 (1.1, 2.6) 104 / 207 0.8 (0.6, 1.1)
VV 2 / 0 -- -- 22 / 35 1.0 (0.6, 1.8)
AV+VV 53 / 47 1.7 (1.1, 2.7) 126 / 242 0.9 (0.7, 1.2)
XPC K939Q
KK 126 / 149 1.0 Ref 103 / 191 1.0 Ref
KQ 91 / 142 0.8 (0.6, 1.2) 148 / 252 1.1 (0.8, 1.5)
QQ 9 / 31 0.3 (0.2, 0.8) 52 / 89 1.1 (0.7, 1.6)
KQ+QQ 100 / 173 0.7 (0.5, 1.0) 200 / 341 1.1 (0.8, 1.5)
RAD23B A249V
AA 203 / 292 1.0 Ref 195 / 327 1.0 Ref
AV 20 / 28 0.9 (0.5, 1.7) 99 / 182 0.9 (0.7, 1.2)
VV -- -- -- 3 / 8 0.7 (0.2, 2.5)
AV+VV 20 / 28 0.9 (0.5, 1.7) 102 / 190 0.9 (0.7, 1.2)
# ‘At-Risk’ Allelesb
0 or 1 49 / 69 1.0 Ref 25 / 49 1.0 Ref
2 or 3 105 / 164 0.9 (0.6, 1.4) 93 / 181 0.9 (0.5, 1.6)
4 or 5 44 / 61 1.0 (0.6, 1.8) 111 / 185 1.1 (0.6, 1.8)
6 or more 6 / 6 1.1 (0.3, 3.9) 42 / 69 1.1 (0.6, 2.0)
a

Adjusted for age, gender and offsets

b

The ‘at-risk’ allele was defined as follows: XPD D312N: N allele; XPD K751Q: Q allele; XPF R415Q: Q allele; XPD D1104H: H allele; XPC A499V: V allele; XPCK939Q: K allele; RAD23B A249V: V allele. The XPC 939 less common allele was associated with reduced risk in this population, thus the more common allele was considered the ‘at-risk’ allele.