Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1023890 1.000 0.080 4 117780291 intergenic variant G/A;C snv 1
rs10905453 1.000 0.080 10 8702058 regulatory region variant A/G;T snv 1
rs11632715 1.000 0.080 15 32712046 intergenic variant G/A snv 0.47 1
rs11694911 1.000 0.080 2 10433072 regulatory region variant C/T snv 0.12 1
rs11986063 1.000 0.080 8 116628076 regulatory region variant C/T snv 0.12 1
rs11987193 1.000 0.080 8 29478491 intergenic variant T/C snv 0.71 1
rs12759486 1.000 0.080 1 221893194 intron variant C/T snv 0.47 1
rs12902616 1.000 0.080 15 32704974 regulatory region variant A/G;T snv 1
rs1583661 1.000 0.080 4 93941116 intergenic variant C/A;T snv 1
rs158552 1.000 0.080 20 54125959 TF binding site variant C/G;T snv 1
rs16888589 1.000 0.080 8 116623363 intergenic variant A/G snv 9.5E-02 1
rs17051076 1.000 0.080 4 130729712 intergenic variant G/A;T snv 4.7E-02 1
rs17217119 1.000 0.080 20 54126051 regulatory region variant A/G snv 0.19 1
rs1870481 1.000 0.080 4 117741865 intergenic variant C/T snv 0.55 1
rs1944682 1.000 0.080 11 121771082 intron variant G/T snv 0.58 1
rs2128383 1.000 0.080 8 129808389 intergenic variant A/G snv 0.15 1
rs2169059 1.000 0.080 4 117786035 intergenic variant C/A snv 0.56 1
rs2170568 1.000 0.080 8 129808129 intergenic variant T/A snv 0.15 1
rs2209907 1.000 0.080 9 80554440 regulatory region variant A/G snv 0.13 1
rs2423297 1.000 0.080 20 7840844 regulatory region variant G/A;C snv 0.34 1
rs27437 1.000 0.080 5 132101268 regulatory region variant A/G snv 0.40 1
rs367615 1.000 0.080 5 109613236 intergenic variant C/G;T snv 1
rs377426 1.000 0.080 4 111841680 intron variant G/T snv 0.55 1
rs4140904 1.000 0.080 4 18314369 intergenic variant A/G snv 0.32 1
rs4574118 1.000 0.080 2 106331987 intergenic variant C/G snv 0.84 1