Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201893408 0.695 0.480 8 93795970 missense variant T/A;C snv 8.0E-06; 1.5E-04 28
rs752362727 0.716 0.480 8 93786255 missense variant C/T snv 2.0E-05 22
rs386834180 0.776 0.360 8 93781725 missense variant T/C snv 2.0E-05 4.2E-05 8
rs863225235 0.790 0.360 8 93782444 missense variant C/A snv 4.0E-06 7.0E-06 7
rs267607119 0.827 0.360 8 93808898 missense variant T/C snv 4.0E-05 8.4E-05 5
rs137853108 0.851 0.320 8 93765617 stop gained A/T snv 1.8E-04 2.6E-04 4
rs202149403 0.851 0.360 8 93780633 missense variant T/C;G snv 8.4E-05 4
rs386834202 0.851 0.320 8 93765574 frameshift variant AG/- del 4.0E-06; 1.9E-04 5.6E-05 4
rs137853107 0.882 0.360 8 93791282 missense variant A/G;T snv 8.0E-06; 4.0E-06 3
rs386834185 0.882 0.320 8 93787843 splice acceptor variant G/C;T snv 3
rs199821258 0.925 0.320 8 93765648 splice donor variant T/G snv 5.6E-05 2.8E-05 2
rs386834182 0.925 0.360 8 93786253 missense variant G/A snv 6.0E-05 4.2E-05 2
rs386834192 0.925 0.320 8 93803685 splice donor variant -/T delins 1.4E-05 2
rs386834205 0.925 0.320 8 93772612 stop gained G/A snv 8.0E-06 7.0E-06 2
rs137853106 1.000 0.280 8 93782456 missense variant A/C snv 1
rs386834181 1.000 0.280 8 93781744 splice donor variant G/- delins 1
rs386834183 1.000 0.280 8 93786256 missense variant G/A;T snv 8.0E-06 1
rs386834184 1.000 0.280 8 93786270 missense variant G/C;T snv 4.0E-06 1
rs386834186 1.000 0.280 8 93791280 frameshift variant AT/- delins 1
rs386834187 1.000 0.280 8 93791320 splice donor variant G/A snv 1
rs386834188 1.000 0.280 8 93755075 missense variant A/G snv 7.0E-06 1
rs386834189 1.000 0.280 8 93797372 missense variant T/C snv 1
rs386834190 1.000 0.280 8 93755776 splice acceptor variant A/- del 9.6E-05 1
rs386834191 1.000 0.280 8 93803662 frameshift variant T/- delins 1
rs386834193 1.000 0.280 8 93804796 missense variant G/A;T snv 8.0E-06; 4.0E-06 1