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Table 1 CARD15 variants in German CHD and control samples

From: Role of NOD2/CARD15 in coronary heart disease

CARD15 variant

CHD

MI

Controls

P(CHD)

P(MI)

R702W (rs2066844)

     

Number of individuals

890

589

632

  

Variant frequency

0.046

0.045

0.055

0.246

0.242

Genotype frequencies

   

0.173

0.290

C/C

0.913

0.914

0.890

  

C/T

0.083

0.083

0.108

  

T/T

0.004

0.003

0.002

  

G908R (rs2066845)

     

Number of individuals

900

596

632

  

Variant frequency

0.017

0.017

0.013

0.476

0.499

Genotype frequencies

   

0.626

0.553

G/G

0.968

0.968

0.973

  

G/C

0.031

0.030

0.027

  

C/C

0.001

0.002

0.000

  

1007fs (rs2066847)

     

Number of individuals

897

594

630

  

Variant frequency

0.027

0.030

0.026

0.736

0.892

Genotype frequencies

   

0.489

0.583

-/-

0.945

0.939

0.942

  

-/insC

0.055

0.061

0.056

  

insC/insC

0.000

0.000

0.002

  
  1. Abbreviations: CHD, coronary heart disease; MI, myocard infarction; insC, cytosine insertion