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Table 1 Genotypes of cases and controls at position SLC26A5 IVS2-2.

From: High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss

Ethnicity

Case Genotypes

Control Genotypes

Fisher's exact test two-tailed p value

 

A/A

A/G

A/A

A/G

  

Hispanic

22

1

75

1

p = 0.41

p = 0.45

Caucasian

34

2

71

3

p = 0.66

 

Uncertain (Caucasian/Mixed Caucasian)

14

1

0

0

Not Done

 

Asian

3

0

50

0

Not Done

 

African American

7

0

46

0

Not Done

 

Total

80

4

242

4

p = 0.12

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