Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12708716 0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs12599402 0.925 0.160 16 11096031 intron variant T/C snv 0.51 2
rs12924729 0.882 0.200 16 11093926 intron variant G/A snv 0.34 2
rs12927355 0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 2
rs13330041 1.000 0.120 16 10994951 intron variant G/A snv 0.25 2
rs17673553 1.000 0.120 16 11148049 intron variant A/G snv 0.18 2
rs2041670 0.851 0.280 16 11080795 intron variant G/A;C snv 2
rs7200786 0.882 0.200 16 11083944 intron variant A/G snv 0.59 2
rs725613 0.851 0.240 16 11075826 intron variant T/G snv 0.42 2
rs12923849 1.000 0.120 16 10968140 intron variant G/A snv 0.13 1
rs12931878 1.000 0.120 16 10948337 intron variant A/G snv 0.14 1
rs17229044 1.000 0.120 16 10969079 intron variant C/T snv 0.16 1
rs2903692 0.807 0.360 16 11144926 intron variant G/A snv 0.33 1
rs9933507 1.000 0.120 16 11107571 intron variant T/C snv 0.46 1
rs998592 0.925 0.160 16 11105821 intron variant C/T snv 0.39 1