Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs4703855 0.827 0.120 5 72398072 regulatory region variant C/T snv 0.24 6
rs4848306 0.851 0.120 2 112840530 non coding transcript exon variant G/A snv 0.39 6
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 6
rs9889296 0.827 0.120 17 34243528 intergenic variant G/A snv 0.33 6
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 5
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 5
rs3129891 0.851 0.160 6 32447303 downstream gene variant G/A snv 0.20 5
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 5
rs6871626 0.851 0.160 5 159399784 intron variant C/A;G snv 0.29 5
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 4
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 4
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 4
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 4
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs7720838 0.925 0.040 5 40486794 intron variant G/T snv 0.52 4
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3