Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
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
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs3794991 1.000 0.080 19 19499787 intron variant C/G;T snv 7.4E-02 5
rs2304130 1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 3
rs7570971 1.000 0.080 2 135080336 intron variant C/A snv 0.61 2