Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs10954213 0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11264799 0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs1310182 0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs13119723 0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs13315591 0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1678542 0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1953126 1.000 0.120 9 120878222 intron variant T/C snv 0.68 3
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs212389 0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 4
rs2221903 0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61