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Table 2 Empirical power for tests at nominal level 0.05 based on 1000 replicates

From: Cohen’s h for detection of disease association with rare genetic variants

Fixed gene length (bp)

Mean no of rare SNPs

 

RD

OR

Cohen’s h

CMC

WSS

VT

250

46.2

    

0.491

0.644

0.501

  

Unadj.

0.142

0.107

0.178

   
  

BH

0.042

0.037

0.051

   
  

Bonf.

0.037

0.030

0.043

   

500

96

    

0.878

0.931

0.882

  

Unadj.

0.465

0.393

0.521

   
  

BH

0.106

0.080

0.135

   
  

Bonf.

0.087

0.064

0.113

   

1000

187.5

    

0.992

0.998

0.992

  

Unadj.

0.584

0.509

0.652

   
  

BH

0.136

0.109

0.162

   
  

Bonf.

0.121

0.083

0.141

   

2000

377.7

    

1

1

1

  

Unadj.

0.880

0.814

0.918

   
  

BH

0.254

0.194

0.306

   
  

Bonf.

0.211

0.143

0.256

   

5000

944.3

    

1

1

1

  

Unadj.

0.973

0.94

0.987

   
  

BH

0.370

0.265

0.451

   
  

Bonf.

0.305

0.191

0.388

   
  1. Unadj.: Without adjustment for multiple testing. BH: Benjamini-Hochberg procedure. Bonf.: Bonferroni correction.