Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72656353 1.000 0.120 17 50185506 missense variant A/G snv 1
rs72656332 0.882 0.120 17 50186895 missense variant C/T snv 3
rs72656320 1.000 0.120 17 50187095 missense variant C/T snv 1
rs1131692320 1.000 0.120 17 50187103 missense variant C/T snv 1
rs67394386 1.000 0.120 17 50188131 missense variant C/A;T snv 3
rs72654795 0.925 0.120 17 50188565 missense variant C/T snv 2
rs67641695 1.000 0.120 17 50188592 missense variant C/T snv 1
rs72653178 0.925 0.120 17 50188619 missense variant C/T snv 2
rs66523073 0.925 0.120 17 50188777 missense variant C/T snv 2
rs72653170 0.752 0.240 17 50188908 missense variant G/A snv 8.0E-06 10
rs67445413 0.925 0.120 17 50189876 missense variant C/A;T snv 2
rs72653131 0.882 0.120 17 50190045 missense variant C/T snv 3
rs67693970 0.882 0.120 17 50190099 missense variant C/G;T snv 3
rs67879854 0.790 0.240 17 50190578 missense variant C/A;T snv 7
rs72651658 0.827 0.200 17 50190861 missense variant C/T snv 7.0E-06 5
rs1114167390 1.000 0.120 17 50191382 splice donor variant C/T snv 1
rs72651645 0.925 0.160 17 50191463 missense variant C/T snv 2
rs67368147 0.925 0.120 17 50191805 missense variant C/A;T snv 2
rs72651642 0.790 0.240 17 50191826 stop gained G/A snv 7.0E-06 7
rs1114167388 1.000 0.120 17 50191840 missense variant C/G snv 1
rs66555264 0.790 0.240 17 50192993 splice donor variant C/A;T snv 7
rs66527965 0.763 0.240 17 50193038 missense variant C/A;T snv 31
rs67682641 0.807 0.240 17 50194375 missense variant C/A;T snv 6
rs66490707 0.790 0.240 17 50195231 splice donor variant C/G;T snv 7
rs72648326 0.790 0.240 17 50195288 stop gained G/A snv 7