Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 6
rs17128183 0.882 0.120 14 55112795 intergenic variant A/G snv 0.57 5
rs7025162 1.000 0.080 9 133290774 regulatory region variant T/C snv 0.82 4
rs10466351 11 92964815 upstream gene variant C/T snv 0.48 3
rs10483639 1.000 0.040 14 54839739 downstream gene variant G/C snv 0.26 3
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 3
rs2040771 22 19174422 downstream gene variant C/A;T snv 3
rs878521 7 44216044 downstream gene variant G/A snv 0.33 3
rs1562064 4 145391948 intergenic variant G/A snv 0.74 2
rs184650103 4 73984932 upstream gene variant C/G;T snv 2
rs34226052 4 88242371 intergenic variant A/G snv 0.22 2
rs61524473 15 45354085 downstream gene variant T/C snv 0.30 2
rs669408 1 232383404 regulatory region variant A/C snv 0.52 2
rs74249229 16 69945368 downstream gene variant C/T snv 4.2E-02 2
rs74331971 8 482881 downstream gene variant G/A snv 1.7E-02 2
rs9411488 9 133278802 upstream gene variant G/T snv 0.34 2
rs9411491 9 133280442 upstream gene variant T/C snv 0.18 2
rs10130783 14 55714800 intergenic variant G/A snv 0.25 1
rs10135789 14 54825302 intergenic variant A/G snv 0.45 1
rs10147667 14 55104131 intergenic variant T/C snv 0.39 1