Table 1 NOD2/CARD15 SNP8, 12 and 13 in patients with sporadic colorectal cancer (CRC) and (CD) and controls
R702W (SNP8) | G908R (SNP 12) | 3020insC (SNP 13) | ||||
|---|---|---|---|---|---|---|
CRC n (%) | Controls n (%) | CRC n (%) | controls n (%) | CRC n (%) | controls n (%) | |
Wild type | 187 (96.4) | 194 (97.0) | 187 (96.4) | 193 (96.5) | 180 (92.8) | 190 (95.0) |
All Carriers | 7 (3.6) | 6 (3.0) | 7 (3.6) | 7 (3.5) | 14 (7.2) | 10 (5.0) |
Heterozygous | 7 (3.6) | 6 (3.0) | 7 (3.6) | 7 (3.5) | 14 (7.2) | 10 (5.0) |
Allele frequency | 7 (1.8) | 6 (1.5) | 7 (1.8) | 7 (1.8) | 14 (3.6) | 10 (2.5) |
P value for carriers | 0.78 | 0.95 | 0.40 | |||
OR carrier (95%CI) | 1.21 (0.39–3.67) | 1.03 (0.35–3.00) | 1.48 (0.64–3.41) | |||