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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