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Table 1 Genotype and allele frequency distribution of LPA SNPs in CAD patients

From: Lack of association between lipoprotein(a) genetic variants and subsequent cardiovascular events in Chinese Han patients with coronary artery disease after percutaneous coronary intervention

Subjects

 

All patients

Patients without MACE, n = 415

Patients with MACE, n = 102

P

N = 517

SNP ID

n (%)

n (%)

n (%)

 

rs6415084

Genotype

    
 

CC

406 (78.5)

367 (78.6)

39 (78.0)

0.250

 

CT

105 (20.3)

94 (20.1)

11 (22.0)

 
 

TT

6 (1.2)

25 (1.3)

0 (0.0)

 
 

Allele

    
 

C

917 (88.7)

828 (85.2)

89 (89.0)

0.302

 

T

117 (11.3)

144 (14.8)

11 (11.0)

 

rs3798220

Genotype

    
 

CC

433 (83.8)

393 (84.2)

40 (68.1)

0.449

 

CG

84 (16.2)

74 (15.8)

10 (21.3)

 
 

Allele

    
 

C

950 (91.9)

860 (91.1)

74 (84.1)

0.870

 

G

84 (8.1)

74(8.9)

14 (15.9)

 

rs10455872

Genotype

    
 

AA

515 (99.6)

465 (99.6)

50 (100.0)

1.000

 

AG

2 (0.4)

2 (0.4)

0 (0.0)

 
 

Allele

    
 

A

1032 (99.8)

932 (99.8)

100 (100.0)

1.000

 

G

2 (0.2)

2 (0.2)

0 (0.0)

 
  1. Abbreviations: CAD coronary artery disease, LPA Lp(a) gene, MACE major adverse cardiovascular event, SNP single nucleotide polymorphism.