Table 2.
Statistical analyses for significant genotype associations
| Patient group | SNP | Genotype | OR | 95% CI | p-value | Stat. Power |
|
| Crohn's disease |
NOD2/CARD15 | Pro268Ser | C/T+T/T T/T |
2.52 12.18 |
1.34 – 4.75 3.86 – 38.37 |
0.005 0.0000003 |
0.59 0.98 |
| NOD2/CARD15 | Arg702Trp | C/T+T/T T/T |
6.65 n/a |
1.99 – 22.17 n/a |
0.0013 n/a |
0.71 n/a |
|
| NOD2/CARD15 | 1007fs | -/C+C/C C/C |
9.59 >16 |
3.94 – 23.29 --- |
0.00000002 0.0006 |
0.99 0.86 |
|
| ATG16L1 | Thr300Ala | T/C+T/T T/T |
0.468 0.632 |
0.24 – 0.90 0.30 – 1.34 |
0.022 0.231 |
0.32 0.05 |
|