Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1317209 0.925 0.120 1 19813543 upstream gene variant G/A;T snv 0.24 2
rs11190140 0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 4
rs11584383 0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs1736135 0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 8