Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs12950743 0.925 0.160 17 39892980 intergenic variant T/C snv 0.45 3
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 3
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 3
rs7359623 0.925 0.160 17 39893336 intergenic variant C/T snv 0.44 3