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Table 3 SNPs that are suggestive as being of genome-wide significance (p < 5 × 10− 6) in univariate and joint analysis*

From: Genome-wide association study for multiple phenotype analysis

SNP

Chr:Pos

Univariate analysis (LMM)

Joint analysis

TG

HDL-C

SSU

mvLMM

USAT

pUSAT

rs90513

1:3189344

3.33E-02

1.20E-06

1.30E-05

7.18E-06

2.36E-05

9.88E-06

rs11940232

4:138953336

6.32E-05

1.98E-05

1.47E-06

8.56E-06

2.65E-06

2.58E-06

rs17058802

4:173880215

5.66E-07

4.56E-03

2.23E-06

3.39E-06

4.13E-06

2.60E-06

rs708010

6:37071350

1.86E-04

4.69E-06

1.01E-06

5.48E-06

2.19E-06

2.12E-06

rs17619780

6:40472303

7.58E-08

2.22E-01

4.95E-06

1.59E-07

9.60E-06

3.01E-07

rs12533593

7:147451966

6.69E-03

2.28E-06

7.72E-06

1.22E-05

1.48E-05

1.01E-05

rs7300117

12:130266575

2.24E-05

8.66E-01

5.60E-04

3.92E-06

9.99E-04

8.58E-06

rs2880301

13:18998534

9.66E-01

7.29E-02

1.95E-01

1.19E-01

1.69E-13

2.22E-01

rs17464499

22:26221715

3.20E-02

4.48E-06

3.02E-05

2.67E-05

6.30E-05

3.29E-05

  1. *pValues of different approaches that reach suggestive genome-wide significance level are in bold