Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs11066301 0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs11085725 0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 3
rs1217393 0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs12531711 0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs13238352 0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 4
rs2283790 0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 3
rs4921283 0.925 0.120 5 160443604 intron variant G/A snv 0.52 2
rs4958880 0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs5029924 0.851 0.200 6 137866361 intron variant C/T snv 0.13 2
rs6568431 0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs6659932 0.827 0.240 1 67336688 intron variant A/C snv 0.81 4
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 4
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs744600 0.851 0.160 2 190700031 intron variant G/T snv 0.60 4
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs76246107 0.851 0.160 19 49618017 intron variant G/A snv 7.7E-02 4
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs802791 0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs911263 0.851 0.200 14 68286876 intron variant C/T snv 0.57 4
rs9603612 0.925 0.120 13 39760715 intron variant C/G snv 0.30 2