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. 2013 Aug 27;12:127. doi: 10.1186/1476-511X-12-127

Table 1.

Genotype and allele frequency distribution of LPA SNPs in CAD patients

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)  

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