From: Frequency and significance of the novel single nucleotide missense polymorphism Val109Asp in the human gene encoding omentin in Caucasian patients with type 2 diabetes mellitus or chronic inflammatory bowel diseases
Total population (n = 190)
Crohn's Disease (n = 131)
Ulcerative Colitis (n = 59)
p
Genotype
Val/Val n (%)
17 (8.9)
11 (8.4)
6 (10.1)
n.s.
Val/Asp n (%)
82 (43.2)
57 (43.5)
25 (42.4)
Asp/Asp n (%)
91 (47.9)
63 (48.1)
28 (47.5)