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. 2012 Feb 14;2012:349469. doi: 10.1155/2012/349469

Table 5.

Number of variant carriers (12333125A>G and 12415557C>T) in CD and UC patients compared to controls.

Category 12333125A>G
Genotype N (a) N (%) of SNP carriers OR (C.I.) P (c) OR (C.I) (b) P (b)
CD Het plus hom 143 28 (19.6) 0.68 (0.40–1–15) 0.15(d) 0.67 (0.40–1.14) 0.14
control Het plus hom 182 48 (26.4)
CD hom 116 1 (0.9) 0.58 (0.05–6.51) 1.0 0.77 (0.23–2.61) 0.68
control hom 136 2 (1.5)

UC Het plus hom 140 30 (21.4) 0.76 (0.45–1.28) 0.31(d) 0.78 (0.46–1.32) 0.35
control Het plus hom 182 48 (26.4)
UC hom 111 1 (0.9) 0.61 (0.06–6.81) 1.0 0.70 (0.21–2.38) 0.57
control hom 136 2 (1.5)

12415557C>T

CD Het plus hom 139 31 (22.3) 0.91 (0.54–1.54) 0.72(d) 0.92 (0.54–1.56) 0.74
control Het plus hom 175 42 (24.0)
CD hom 109 1 (0.9) 0.31 (0.03–2.80) 0.39 0.54 (0.18–1.62) 0.27
control hom 137 4 (2.9)

UC Het plus hom 134 32 (23.9) 0.99 (0.59–1.68) 0.98(d) 0.94 (0.55–1.62) 0.83
control Het plus hom 175 42 (24.0)
UC hom 104 2 (1.9) 0.65 (0.12–3.63) 0.70 0.84 (0.35–1.99) 0.69
control hom 137 4 (2.9)

OR: odds ratio; CI: confidence interval; N: absolute number; het: heterozygous; hom: homozygous; (a)absolute number of all patients of the respective subgroup included into the analysis; (b)adjusted for age and sex; (c) P values calculated with Fisher's exact test; (d) P value calculated with Chi-Square test.