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Table 3 Significant SNPs for CAD under different ES measures at genome-wide significance levels

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

Type of SNPs

Significant SNPs

OR

RD

Cohen’s h

Common

Number

26

26

26

 

Median

1.327

0.065

0.134

 

Range

(0.757, 6.104)

(-0.063, 0.354)

(-0.129, 0.795)

Rare

Number

9

13

18

 

Median

2.144

0.021

0.119

 

Range

(1.88, 2.41)

(-0.009, 0.038)

(-0.167, 0.179)