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Table 6 Genotype distribution of the Val109Asp SNP in 190 patients suffering from chronic inflammatory bowel diseases

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)

n.s.

Asp/Asp n (%)

91 (47.9)

63 (48.1)

28 (47.5)

n.s.

  1. n.s. not significant between groups