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Table 2 Frequency of gene polymorphisms in two groups

From: Association of NPC1L1 and HMGCR gene polymorphisms with coronary artery calcification in patients with premature triple-vessel coronary disease

Gene

SNP

Genotype

High-degree CAC

(n = 173)

Low-degree CAC

(n = 699)

P value

NPC1L1

rs11763759

TT

153 (88.4%)

622 (89.1%)

0.587

CT

20 (11.6%)

71 (10.2%)

CC

0 (0.0%)

5 (0.7%)

 

rs4720470

CC

75 (43.6%)

340 (48.6%)

0.402

 

CT

78 (45.3%)

278 (39.8%)

 

TT

19 (11.0%)

81 (11.6%)

 

rs2072183

GG

64 (37.0%)

278 (39.9%)

0.577

 

CG

81 (46.8%)

326 (46.8%)

 

CC

28 (16.2%)

93 (13.3%)

 

rs2073547

AA

64 (37.0%)

276 (39.5%)

0.668

 

GA

81 (46.8%)

327 (46.8%)

 

GG

28 (16.2%)

96 (13.7%)

HMGCR

rs12916

TT

40 (23.3%)

172 (24.7%)

0.302

TC

89 (51.7%)

317 (45.5%)

CC

43 (25.0%)

208 (29.8%)

 

rs2303151

CC

118 (68.2%)

440 (62.9%)

0.424

 

CT

48 (27.7%)

229 (32.8%)

 

TT

7 (4.0%)

30 (4.3%)

 

rs4629571

AA

149 (86.1%)

570 (81.5%)

0.387

 

AG

22 (12.7%)

120 (17.2%)

 

GG

2 (1.2%)

9 (1.3%)

  1. CAC: coronary artery calcification; SNP: single nucleotide polymorphisms; NPC1L1: Niemann-Pick C1-like 1; HMGCR: 3-hydroxy-3-methylglutaryl-coenzyme A reductase