Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137929307 0.752 0.240 19 11116928 missense variant G/A snv 4.4E-05 4.9E-05 10
rs139043155 0.790 0.200 19 11106668 missense variant T/A snv 3.2E-05 4.2E-05 10
rs28942084 0.763 0.200 19 11120436 missense variant C/A;T snv 2.8E-05 4.2E-05 9
rs750518671 0.790 0.200 19 11128085 missense variant G/A;C;T snv 8.0E-06 9
rs28942080 0.807 0.200 19 11113743 missense variant G/A;C;T snv 1.2E-05; 4.0E-06 8
rs570942190 0.827 0.200 19 11113337 missense variant C/T snv 2.4E-05 7.0E-06 7
rs879254838 0.827 0.120 19 11113314 missense variant A/C;T snv 7
rs879254965 0.827 0.200 19 11116140 missense variant G/A;C;T snv 7
rs879255051 0.827 0.120 19 11120091 splice acceptor variant G/A;C snv 7
rs879255193 0.851 0.120 19 11129512 splice acceptor variant G/A;C snv 6
rs13306512 0.882 0.120 19 11107513 stop gained C/A;G;T snv 4.0E-06; 2.0E-05 5
rs752935814 0.882 0.120 19 11120380 stop gained G/A;C snv 5
rs769370816 0.882 0.120 19 11116125 missense variant G/A;T snv 8.0E-06 5