Table 2 of Awadalla, Mol Vis 2011; 17:2248-2254.


Table 2. Genotype counts (n) and frequencies (%) of HGF SNPs in Nepalese samples and p-value for association under the allelic model, bold p-values are considered significant after bonferroni correction (p<0.004).

SNP Genotype Case n (%) Control n (%) p-value Adjusted p-value* Odds ratio (95% CI)
rs5745752 AA 16 (16.0) 30 (15.0) 0.754 0.694 0.9 (0.7–1.3)
  AG 44 (41.0) 90 (44.0)      
  GG 46 (43.0) 82 (41.0)      
rs5745718 AA 5 (4.0) 3 (1.0) 0.002 0.003 2.2 (1.3–3.5)
  AC 27 (26.0) 30 (15.0)      
  CC 71 (70.0) 163 (84.0)      
rs12536657 AA 5 (4.0) 3 (1.0) 0.002 0.009 2.1 (1.3–3.3)
  AG 29 (28.0) 34 (17.0)      
  GG 71 (68.0) 165 (82.0)      
rs2286194 AA 4 (4.0) 8 (4.0) 0.480 0.453 0.9 (0.6–1.3)
  AT 28 (26.0) 62 (31.0)      
  TT 74 (70.0) 132 (65.0)      
rs5745692 CC 0 (0.0) 1 (1.0) 0.139 0.998 0.2 (0.03–1.9)
  CG 1 (1.0) 6 (3.0)      
  GG 105 (99.0) 196 (96.0)      
rs12540393 CC 5 (5.0) 3 (3.0) 0.0006 0.001 2.2 (1.4–3.5)
  CT 34 (32.0) 37 (18.0)      
  TT 67 (63.0) 162 (79.0)      
rs17427817 CC 5 (5.0) 3 (2.0) 0.0006 0.001 2.2 (1.4–3.5)
  CG 34 (32.0) 37 (18.0)      
  GG 67 (63.0) 162 (80.0)      
rs12707453 GG 3 (3.0) 12 (6.0) 0.749 0.784 0.9 (0.6–1.4)
  GA 42 (40.0) 73 (36.0)      
  AA 60 (57.0) 117 (58.0)      
rs5745616 AA 16 (15.0) 21 (10.0) 0.540 0.469 1.1 (0.8–1.6)
  AG 43 (41.0) 91 (45.0)      
  GG 47 (44.0) 90 (45.0)      
rs3735520 TT 15 (14.0) 38 (19.0) 0.236 0.134 0.8 (0.6–1.1)
  TC 49 (47.0) 96 (47.0)      
  CC 41 (39.0) 68 (34.0)      
rs6942495 GG 22 (21.0) 51 (26.0) 0.745 0.878 0.9 (0.7–1.3)
  GC 56 (53.0) 95 (47.0)      
  CC 27 (26.0) 55 (27.0)      
rs17501080 CC 3 (3.0) 2 (1.0) 0.569 0.863 1.2 (0.7–2.0)
  CA 19 (18.0) 38 (19.0)      
  AA 83 (79.0) 162 (80.0)