Table 1:

SNPs identified by DSILT to interact with the statin genetic variants rs17238484-G on the risk for T2D. The second column presents the name of the gene where the SNP locates. The third column presents the minor allele frequency (MAF) of each SNP averaged over the three sites. The last three columns respectively present the $p$–values obtained using One–shot approach with all the $M=6$ studies, One–shot with solely the datasets ${\text{MVP}}_f$ and ${\text{MVP}}_m$ and the proposed method with all the $M=6$ studies. The $p$–values shown in black fonts represent the SNPs selected by each method.

SNP	Gene	MAF	One–shot	MVP–only	DSILT
rs12328675-T	COBLL1	0.13	1.1×10−3	2.3 × 10−3	6.0×10−4
rs2200733-T	LOC729065	0.18	3.7 × 10−2	5.7 × 10−3	6.2×10−4
rs581080-G	TTC39B	0.22	3.6×10−6	1.1×10−6	2.6×10−6
rs35011184-A	TCF7L2	0.22	1.9 × 10−2	5.2 × 10−2	8.6×10−4
rs838880-T	SCARB1	0.36	6.7×10−4	6.0×10−5	6.2×10−4