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
rs202149403 0.851 0.360 8 93780633 missense variant T/C;G snv 8.4E-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
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
rs386834189 1.000 0.280 8 93797372 missense variant T/C snv 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
rs386834195 1.000 0.280 8 93808942 stop gained G/T snv 1
rs386834196 1.000 0.280 8 93809057 stop gained A/T snv 1
rs386834197 1.000 0.280 8 93809056 frameshift variant -/A delins 1
rs386834198 1.000 0.280 8 93809811 frameshift variant -/TA delins 1
rs386834199 1.000 0.280 8 93815437 missense variant T/C snv 4.0E-06 1
rs386834200 1.000 0.280 8 93758552 frameshift variant AC/- delins 1
rs386834203 1.000 0.280 8 93765574 frameshift variant A/- del 1
rs386834204 1.000 0.280 8 93765642 frameshift variant A/- delins 1
rs386834206 1.000 0.280 8 93780612 missense variant C/T snv 1
rs386834207 1.000 0.280 8 93780872 splice acceptor variant A/G snv 1
rs386834208 1.000 0.280 8 93780892 missense variant G/T snv 8.0E-06 1