Table 8 Comparison of patients and controls who are homozygous wild type for the IGR2198a_1 IBD5 haplotype marker single nucleotide polymorphism but have a risk allele in the TC haplotype.
Subjects with no IBD5 risk alleles | Subjects with TC haplotype but no IBD5 risk alleles | |
---|---|---|
Controls | 82 | 10 |
IBD patients | 72 | 5 |
χ2 p value comparing IBD patients with controls | 0.27 | |
CD patients | 47 | 4 |
χ2 p value comparing CD patients with controls | 0.57 | |
UC patients | 18 | 0 |
χ2 p value comparing UC patients with controls | 0.20 |
The TC haplotype does not show an independent effect on disease susceptibility of the three IBD5 marker SNPs IGR2096a_1, IGR2198a_1, and IGR2230a_1, examined either individually or when combined in patients with IBD, Crohn's disease, or ulcerative colitis compared with controls. The data shown are only for IGR2198a_1, but results for all SNPs were non‐significant and are available on request.
CD, Crohn's disease; IBD, inflammatory bowel disease; SNP, single nucleotide polymorphism; UC, ulcerative colitis.