Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
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
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
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
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
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2221903 0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs2488457 0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs26232 0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs3087456 0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs3093023 0.851 0.160 6 167120802 intron variant G/A snv 0.34 7
rs34933034
CSK
0.925 0.120 15 74787133 intron variant G/A;T snv 3
rs3761847 0.827 0.200 9 120927961 intron variant G/A snv 0.52 8
rs3761959 0.827 0.320 1 157699488 intron variant C/A;G;T snv 7
rs3890745 0.925 0.200 1 2622185 intron variant T/C snv 0.40 4