Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1214611 0.925 0.200 1 167479867 intron variant A/G snv 0.54 2
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs12660382 0.882 0.200 6 31475546 intron variant C/T snv 0.19 3
rs12708716 0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs12917716 0.851 0.200 16 11095291 intron variant G/C snv 0.51 4
rs13199524 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 9
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1678542 0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs17388568 0.827 0.280 4 122408207 intron variant G/A snv 0.20 6
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1980493 0.776 0.400 6 32395438 intron variant T/C snv 0.13 10
rs204990 0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs204991 0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs206015 0.925 0.200 6 32214982 intron variant G/A snv 0.15 2
rs2064478 0.925 0.200 6 33104489 intron variant C/T snv 0.28 2
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2156875 0.882 0.200 6 31349570 intron variant C/T snv 0.50 6
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20