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. 2018 Sep 17;12(Suppl 9):55. doi: 10.1186/s12919-018-0135-8

Table 3.

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

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