Table 4.
Variant | p.Arg702Trp | p.Gly908Arg | p.Leu1007fsinsC | WT |
p.Arg702Trp | 2/0/4 | 1/0/1 | 2/1/1 | 6/1/2 |
p.Gly908Arg | 0/0/0 | 1/0/0 | 3/1/3 | |
p.Leu1007fsinsC | 0/0/0 | 1/1/1 | ||
WT | 70/42/102 |
In each cell of the table, the genotype is obtained by combining the two genetic variants indicated in the corresponding row and column. No patients homozygous for NOD2 gene p.Gly908Arg and p.Leu1007fsinsC mutations were found in this study. CD: Crohn's disease; UC: Ulcerative colitis; HC: Healthy controls; WT: Wild type.