Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11074956 0.925 0.160 16 11243864 downstream gene variant G/T snv 0.34 2
rs12979659 0.925 0.160 19 6825021 intron variant T/C snv 0.36 0.28 2
rs151719 0.925 0.160 6 32936123 non coding transcript exon variant C/T snv 0.72 2
rs17421624 0.925 0.160 6 32098400 intron variant T/C snv 0.25 2
rs2157051 0.925 0.160 6 32690847 regulatory region variant G/A snv 0.69 2
rs2524095 0.925 0.160 6 31298340 intron variant A/C snv 0.65 2
rs2546133 0.925 0.160 19 6799666 intron variant T/A;C snv 2
rs2617822 0.925 0.160 19 6801470 intron variant G/A;C snv 2
rs2621383 0.925 0.160 6 32791558 intergenic variant C/A snv 0.65 2
rs2621384 0.925 0.160 6 32791496 intergenic variant C/T snv 0.66 2
rs2849015 0.925 0.160 6 32231159 intergenic variant G/A snv 0.38 2
rs2857161 0.925 0.160 6 32791520 intergenic variant G/A snv 0.65 2
rs2894249 0.925 0.160 6 32358058 intron variant C/G;T snv 2
rs3129872 0.925 0.160 6 32439376 upstream gene variant A/T snv 0.24 2
rs3129877 0.925 0.160 6 32440820 intron variant G/A snv 0.26 2
rs3135342 0.925 0.160 6 32428838 intergenic variant G/T snv 0.24 2
rs3135377 0.925 0.160 6 32417622 regulatory region variant A/G snv 0.80 2
rs3135392 0.925 0.160 6 32441465 intron variant C/A snv 0.38 2
rs404890 0.925 0.160 6 32231090 intergenic variant C/A snv 0.35 2
rs486416 0.925 0.160 6 31888293 intron variant G/A snv 0.77 0.76 2
rs6684865 0.925 0.160 1 2614790 intron variant G/A snv 0.40 2
rs682626 0.925 0.160 19 6774058 intron variant G/A;T snv 2
rs793108 0.925 0.160 10 31126177 intron variant C/T snv 0.40 2
rs9267873 0.925 0.160 6 32231575 intergenic variant C/G;T snv 2
rs9268429 0.925 0.160 6 32377275 intron variant A/G snv 0.24 2