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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