Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 26
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 22
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 19
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 13
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 12
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 10
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 9
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 9
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 8
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 8
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 8
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 7
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 7
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 7
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 7
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 7
rs10509291 0.827 0.280 10 67875446 downstream gene variant T/A snv 7.1E-02 6
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 6