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. 2006 Jun 5;103(24):9256–9261. doi: 10.1073/pnas.0603485103

Table 3.

Distribution of the ERCC6 (rs3793784) and CFH (rs380390) SNP types and the combined effect on the disease risk

ERCC6–C6530>G CFH rs380390
Control (n = 268)
Case (n = 460)
OR (CI)
GG GC CC GG GC CC GG GC CC
CC 45 (16.8%) 53 (19.8%) 16 (6.0%) 33 (7.2%) 66 (14.4%) 50 (10.9%) Reference 1.65 (0.90–3.03) 4.29* (2.02–9.09)
CG 43 (16.0%) 56 (20.9%) 20 (7.5%) 42 (9.1%) 94 (20.4%) 102 (22.2%) 1.24 (0.65–2.38) 2.17 (1.20–3.90) 7.70* (3.86–15.34)
GG 16 (6.0%) 17 (6.3%) 2 (0.8%) 8 (1.7%) 31 (6.7%) 34 (7.4%) 0.62 (0.23–1.69) 2.64 (1.22–5.75) 23.05** (5.07–104.78)

CI, 95% confidence interval. Reference, cell was taken as the baseline for the indicated statistical calculation. ∗, P < 0.0001, using CC/GG as the reference. ∗∗, P < 0.0001, using CC/GG as reference or P < 0.05, using CC/CC (two-tailed) or CG/CC (one-tailed) as the references.