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Table 3 Genotype, allele frequencies and risk of MI associated with rs599839 and rs646776 in the SHEEP

From: Chromosome 1p13 genetic variants antagonize the risk of myocardial infarction associated with high ApoB serum levels

   MI   P
   Cases/Controls   
rs599839 AA 779/1035   
  AG 340/431   
  GG 33/33   0.5
Allele G   0.18/0.17   0.5
   Crude Adjusted  
   OR (95%CI) OR (95%CI)  
Additive   1.08 (0.93-1.26) 1.10 (0.93-1.30)  
Dominant   1.07 (0.91-1.27) 1.10 (0.91-1.33)  
Recessive   1.36 (0.79-2.13) 1.23 (0.69-2.17)  
rs646776     
  TT 686/875   
  CT 413/561   
  CC 58/70   0.7
Allele C   0.23/0.23   0.8
   Crude Adjusted  
   OR (95%CI) OR (95%CI)  
Additive   0.97 (0.85-1.11) 0.97 (0.84-1.13)  
Dominant   0.95 (0.82-1.11) 0.94 (0.78-1.12)  
Recessive   1.07 (0.75-1.53) 1.15 (0.76-1.73)