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Table 3 Association results for the genotyped exonic variants with clinical and subclinical CVD and blood lipids

From: Analysis of common and coding variants with cardiovascular disease in the diabetes heart study

  

Additive

Dominant

Recessive

SNP

Trait

P-value

β value

SE

P-value

β value

SE

P-value

β value

SE

rs3135506

Triglycerides

5×10 −5

0.189

0.465

3×10−4

0.17

0.31

7×10−4

0.93

0.27

rs3135506

LDL

0.0012

−9.48

2.92

7×10−4

−10.1

2.99

0.65

10.1

22.4

rs3135506

HDL

0.0066

−0.20

0.07

0.011

−0.19

0.07

0.13

−0.63

0.42

rs651821

Triglycerides

8×10−4

0.15

0.04

0.004

0.14

0.05

0.005

0.5

0.18

rs651821

History of CVD

0.02

0.27

0.11

0.08

0.23

0.13

0.009

1.29

0.56

rs138326449

Triglycerides

0.0017

−0.97

0.31

0.0017

−0.97

0.31

NA

NA

NA

rs138326449

HDL

0.13

1.16

0.46

0.013

1.16

0.46

NA

NA

NA

rs45456595

IMT

0.0022

0.07

0.02

0.0022

0.07

0.02

NA

NA

NA

rs5128

Triglycerides

0.0096

0.10

0.04

0.03

0.09

0.04

0.01

0.41

0.16

rs72650673

Triglycerides

0.0084

0.77

0.29

0.0084

0.77

0.29

NA

NA

NA

  1. Associations were examined under additive, dominant and recessive genetic models. Bold indicates statistical significance. History of CVD = prior reports of CVD events, IMT = carotid intima-media thickness, SE = standard error.