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. 2006 Jul 20;108(9):3161–3167. doi: 10.1182/blood-2005-01-026690

Table 3.

Risk of NHL in relation to variants in DNA repair genes, by repair pathway

Variants according to gene Cases Controls OR (95% CI) P trend
Nonhomologous end joining/V(D)J genes
    LIG4 (T9I)
        CC 792 628 1.0
        CT 300 275 0.9 (0.7-1.1)
        TT 18 28 0.5 (0.3-0.9) .03
        CT or TT 318 303 0.8 (0.7-1.0)
    RAG1 (K820R)
        AA 814 722 1.0
        AG 256 185 1.3 (1.0-1.6)
        GG 35 15 2.7 (1.4-5.0) < .001
        AG or GG 291 200 1.4 (1.1-1.7)
Homologous recombination repair
    BRCA2 (N372H)
        AA 577 505 1.0
        AC 441 361 1.1 (0.9-1.3)
        CC 98 60 1.5 (1.0-2.1) .07
        CC or AC 539 421 1.1 (0.9-1.3)
    WRN (V114I)
        GG 652 533 1.0
        GA 86 91 0.8 (0.6-1.1)
        AA 5 9 0.4 (0.1-1.3) .04
        GA or AA 91 100 0.7 (0.6-1.0)
Base excision repair
    XRCC1 (R194W)
        CC 916 804 1.0
        CT 186 116 1.4 (1.1-1.8)
        TT 9 7 1.3 (0.5-3.4) .007
        CT or TT 195 123 1.4 (1.1-1.8)

All analyses were adjusted for reference age (younger than 55 years, 55 to 64 years, 65 years or older), sex, race (White, African American, other), and study site. Participants with missing data are omitted.

OR indicates odds ratio; CI, confidence interval.