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Table 3 Association of CYP7B1 polymorphisms with CHD risk

From: The effect of CYP7B1 polymorphisms on the risk of coronary heart disease in Hainan Han population

SNP ID Model Allele/Genotype Case N Control N OR (95% CI) p
rs7836768 Allele A 595 616 1  
   G 419 404 1.07 (0.90–1.28) 0.431
  Codominant AG 239 71 0.90 (0.69–1.19) 0.464
   GG 90 262 1.27 (0.87–1.84) 0.220
   AA 178 177 1  
  Dominant AG-GG 329 333 0.98 (0.76–1.27) 0.878
  Recessive AA-AG 417 248 1  
   GG 90 262 1.34 (0.96–1.89) 0.090
  Log-additive 1.08 (0.90–1.29) 0.427
rs6472155 Allele A 725 751 1  
   G 291 269 1.12 (0.92–1.36) 0.252
  Codominant AG 219 215 1.08 (0.83–1.39) 0.575
   GG 36 27 1.39 (0.82–2.35) 0.226
   AA 253 268 1  
  Dominant AG-GG 255 242 1.11 (0.87–1.42) 0.404
  Recessive AA-AG 472 483 1  
   GG 36 27 1.34 (0.80–2.25) 0.265
  Log-additive 1.12 (0.92–1.38) 0.260
rs2980003 Allele C 653 666 1  
   T 363 352 1.05 (0.88–1.26) 0.587
  Codominant TC 233 230 1.05 (0.81–1.37) 0.722
   TT 65 61 1.09 (0.73–1.63) 0.663
   CC 210 218 1  
  Dominant TC-TT 298 291 1.06 (0.82–1.36) 0.657
  Recessive CC-TC 443 448 1  
   TT 65 61 1.07 (0.73–1.55) 0.738
  Log-additive 1.05 (0.87–1.26) 0.626
  1. CI, confidence interval; OR, odds ratio; SNP: single nucleotide polymorphism; OR, Odds ratio, 95% CI; 95% confidence intervals
  2. p‐values were calculated by unconditional logistic regression analysis with adjustment for age and gender
  3. p < 0.05 indicates statistical significance