Table 3.
Mutant | Genotype | Allele | Control |
CD |
UC |
||
P value | P value | ||||||
P268S | aP1 | NS1 | |||||
CC | 71 (98.6) | 42 (87.5) | 54 (100.0) | ||||
CT | 1 (1.4) | 6 (12.5) | 0 (0.0) | ||||
TT | 0 (0.0) | 0 (0.0) | 0 (0.0) | ||||
T | 1 (0.7) | 6 (6.2) | cP2 | 0 (0.0) | NS2 | ||
JW1 | NS1 | NS1 | |||||
CC | 72 (100.0) | 48 (100.0) | 54 (100.0) | ||||
CT | 0 (0.0) | 0 (0.0) | 0 (0.0) | ||||
TT | 0 (0.0) | 0 (0.0) | 0 (0.0) | ||||
T | 0 (0.0) | 0 (0.0) | NS2 | 0 (0.0) | NS2 | ||
N852S | NS1 | NS1 | |||||
AA | 72 (100.0) | 48 (100.0) | 54 (100.0) | ||||
AG | 0 (0.0) | 0 (0.0) | 0 (0.0) | ||||
GG | 0 (0.0) | 0 (0.0) | 0 (0.0) | ||||
G | 0 (0.0) | 0 (0.0) | NS2 | 0 (0.0) | NS2 |
Comparisons of genotype frequencies;
Comparisons of allele frequencies.
P < 0.05 vs control using Fisher's exact test;
P < 0.05 vs control using Fisher's exact test. CD: Crohn’s disease; UC: Ulcerative colitis; NS: No significance.