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Table 3 The association between 4 SNPs within VDR gene and RCC risk

From: Vitamin D receptor gene polymorphisms and its interactions with environmental factors on renal cell carcinoma risk

SNP

Genotypes and Alleles

Frequencies N (%)

OR (95 %CI) a

HWE test for controls

Controls (n = 735)

Cases (n = 366)

rs2228570 (FokI)

    

0.997

 

CC

432 (58.8)

191 (52.2)

1.00 (ref)

 
 

CT

263 (35.8)

143 (39.1)

1.32 (0.91–1.83)

 
 

TT

40 (5.4)

32 (8.7)

1.55 (0.72–2.42)

 
 

CT + TT

303 (41.2)

175 (47.8)

1.39 (0.86–1.93)

 
 

Allele, T (%)

343 (23.3)

207 (28.3)

  

rs7975232 (ApaI)

    

0.289

 

CC

475 (64.6)

182 (49.7)

1.00 (ref)

 
 

CA

226 (30.7)

149 (40.7)

1.63 (1.21–2.04)

 
 

AA

34 (4.6)

35 (9.6)

2.02 (1.47–2.62)

 
 

CA + AA

260 (35.4)

184 (50.3)

1.75 (1.26–2.28)

 
 

Allele, A (%)

294 (20.0)

219 (29.9)

  

rs731236 (TaqI)

    

0.735

 

TT

460 (62.6)

200 (54.6)

1.00 (ref)

 
 

TC

241 (32.8)

139 (38.0)

1.24 (0.92–1.65)

 
 

CC

34 (4.6)

27 (7.4)

1.31 (0.81–1.86)

 
 

TC + CC

275 (37.4)

166 (45.4)

1.26 (0.89–1.69)

 
 

Allele, C (%)

309 (21.0)

193 (26.4)

  

rs1544410 (BsmI)

    

0.655

 

GG

466 (63.4)

211 (57.7)

1.00 (ref)

 
 

GA

236 (32.1)

130 (35.5)

1.31 (0.87–1.79)

 
 

AA

33 (4.5)

25 (7.8)

1.45 (0.78–2.15)

 
 

GA + AA

269 (36.6)

155 (42.3)

1.34 (0.84–1.87)

 
 

Allele, A (%)

302 (20.5)

180 (24.6)

  
  1. aAdjusted for gender, age, hypertension, diabetes, smoking, alcohol drinking and BMI