Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs4788084 0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 3
rs12722495 0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1
rs1004446 0.827 0.240 11 2148913 intron variant G/A snv 0.37 3
rs3788013 0.851 0.240 21 42421219 intron variant C/A snv 0.44 1
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs689 0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 1
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs12708716 0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs11755527 0.851 0.360 6 90248512 intron variant C/G snv 0.36 3
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs4689388 0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs2292239 0.742 0.480 12 56088396 intron variant T/G snv 0.65 4
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13