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Table 3 Genotype frequencies of the Behçet's disease-associated single-nucleotide polymorphisms identified in this study

From: Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study

   Number   
SNP Genotype Cases Controls OR (95% CI) P value
rs11206377 GG 62 36 2.29 (1.39–3.78) 0.0011 (GG versus AG+AA)
  AG 66 77   
  AA 16 32   
rs2061634 GG 32 8 4.79 (2.13–10.77) 0.000047 (GG versus CG+CC)
  CG 66 66   
  CC 56 80   
rs317711 CC 12 3 4.23 (1.17–15.32) 0.018 (CC versus GC+GG)
  GC 53 34   
  GG 85 112   
rs4936742 TT 47 23 2.60 (1.48–4.59) 0.00076 (TT versus CT+CC)
  CT 67 79   
  CC 28 42   
rs9513584 GG 32 14 2.69 (1.37–5.29) 0.0033 (GG versus AG+AA)
  AG 66 70   
  AA 47 63   
  1. Odds ratios (ORs) and P values were calculated for the frequency of the homozygous-risk genotype in patients compared with controls. CI, confidence interval; SNP, single-nucleotide polymorphism.