Allele frequency % | Significance CD v controls | ||||
---|---|---|---|---|---|
SNP | CD | UC | Controls | p Value | RR (95% CI) |
IBD, inflammatory bowel disease; SNP, single nucleotide polymorphism; CD, Crohn’s disease; UC, ulcerative colitis; RR, relative risk. | |||||
p values in bold are significant (p<0.05) after Bonferroni correction factor of three (number of SNPs tested for association). | |||||
IGR2060a_1 C | 52.1 | 43.7 | 43.3 | 0.0001 | 1.4 (1.2–1.7) |
IGR2198a_1 G | 50.8 | 42.9 | 42.0 | 0.0001 | 1.4 (1.2–1.7) |
IGR3096a_1 C | 58.0 | 49.1 | 48.7 | <0.0001 | 1.5 (1.2–1.7). |