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Table 3 The distribution of affected alleles of SLC26A4 c.919-2A > G was found in patients with NSHL in nine different areas of Yunnan

From: Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China

Gene

Variant

Number of Affected Alleles

Total patients

Han Chinese group

Minority group

χ2

P

OR (95%CI)

(n = 1167)

(n = 533)

(n = 634)

(frequencies)

(frequencies)

(frequencies)

SLC26A4

c.919-2A > G

Homozygous

8 (0.69%)

5 (0.94%)

3 (0.47%)

0.363

0.547

1.992 (0.474, 8.373)

  

Heterozygous

25 (2.14%)

19 (3.56%)

6 (0.95%)

9.470

0.002

3.869 (1.534, 9.759)

  

Total carrier rate

33 (2.83%)

24 (4.50%)

9 (1.42%)

10.018

0.002

3.274 (1.509, 7.107)

  

Allele G

41(1.76%)

29(2.72%)

12 (0.95%)

10.562

0.001

2.927 (1.486, 5.765)

 

c.2168 A > G

Homozygous

1 (0.09%)

0 (0.00%)

1 (0.16%)

——

1.000

——

  

Heterozygous

7 (0.60%)

5 (0.94%)

2 (0.32%)

0.983

0.321

0.334(0.065, 1.729)

  

Total carrier rate

8 (0.69%)

5 (0.94%)

3 (0.47%)

0.363

0.547

0.502(0.119, 2.111)

  

Allele G

9(0.40%)

5 (0.47%)

4 (0.32%)

0.068

0.794

0.670(0.179, 2.510)