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Table 2 Associations of candidate SNPs with the risk of NIHL

From: Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study

Gene

SNP

Genotype

Control n (%)

Case n (%)

P-value

OR (95 % CI)a

EYA4

rs3777781

TT

137 (29.2)

166 (35.2)

 

1

 

AT

236 (50.3)

235 (49.8)

0.116

0.759 (0.539, 1.070)

 

AA

96 (20.5)

71 (15.0)

0.015

0.570 (0.363, 0.895)

 

Ptrend

  

0.019

 
 

AT/AA

332 (70.8)

306 (64.8)

0.047

0.721 (0.522, 0.996)

rs212769

GG

354 (75.2)

336 (71.0)

 

1

 

AG

112 (23.8)

129 (27.3)

0.062

1.395 (0.984,1.979)

 

AA

5 (1.1)

8 (1.7)

0.214

2.369 (0.608,9.234)

 

Ptrend

  

0.033

 
 

AG/AA

117 (24.8)

137 (29.0)

0.041

1.430 (1.014,2.016)

GRHL2

rs666026

TT

244 (51.9)

222 (47.0)

 

1

 

GT

186 (39.6)

204 (43.2)

0.118

1.287 (0.938,1.767)

 

GG

40 (8.5)

46 (9.7)

0.121

1.554 (0.891,2.71)

 

Ptrend

  

0.051

 
 

GT/GG

226 (48.1)

250 (53.0)

0.065

1.329 (0.983,1.798)

DFNA5

rs2521768

TT

289 (61.4)

305 (64.6)

0.158

1

 

CT

155 (32.9)

148 (31.4)

0.249

0.825 (0.595,1.144)

 

CC

27 (5.7)

19 (4.0)

0.089

0.524 (0.249,1.104)

 

Ptrend

  

0.065

 
 

CT/CC

182 (38.6)

167 (35.4)

0.124

0.782 (0.571, 1.070)

rs2521758

TT

450 (95.5)

458 (97.0)

 

1

 

GT

20 (4.2)

14 (3.0)

0.078

0.474 (0.206,1.088)

 

GG

1 (0.2)

0 (0.0)

1.000

 
 

GT/GG

21 (4.5)

14 (3.0)

0.052

0.441 (0.194,1.006)

  1. acalculated with logistic regression adjusted by age, CNE, smoking, drinking