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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)

 
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