Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs660895 0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs10947261 0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs13192471 0.925 0.160 6 32703326 downstream gene variant T/C snv 0.19 3
rs7765379 0.827 0.280 6 32713151 upstream gene variant T/G snv 0.10 3
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 3
rs1063355 0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 2
rs9267911 0.925 0.160 6 32237333 intergenic variant T/C snv 0.45 2