Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4