Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 15
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 10
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 8
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 7
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 6
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 4
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 4
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 3
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 3
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 3
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 2
rs16969681 0.776 0.080 15 32700910 downstream gene variant C/T snv 0.11 2
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 2
rs4813802 0.776 0.080 20 6718948 regulatory region variant T/G snv 0.28 2
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 1
rs1367374 0.790 0.080 2 153074663 intergenic variant G/C snv 0.19 1
rs16941835 0.790 0.080 16 86662114 intron variant G/C snv 0.20 1
rs2423279 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 1
rs6061231 0.790 0.080 20 62381861 downstream gene variant C/A snv 0.28 1
rs6469656 0.790 0.080 8 116635549 regulatory region variant G/A;C snv 1
rs72647484 0.790 0.080 1 22261235 regulatory region variant T/C snv 6.2E-02 1
rs964293 0.790 0.080 20 54200178 TF binding site variant C/A;T snv 1
rs1254244346 1.000 0.080 9 104822502 missense variant G/A snv 4.0E-06 1
rs11169552 0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 2