Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800250 1.000 0.120 7 94427801 missense variant A/C snv 1
rs72656353 1.000 0.120 17 50185506 missense variant A/G snv 1
rs72659345 1.000 0.120 7 94430291 frameshift variant ATAA/- delins 1
rs72667031 0.925 0.120 17 50197983 missense variant C/A snv 2
rs66527965 0.763 0.240 17 50193038 missense variant C/A;T snv 31
rs66555264 0.790 0.240 17 50192993 splice donor variant C/A;T snv 7
rs67879854 0.790 0.240 17 50190578 missense variant C/A;T snv 7
rs67682641 0.807 0.240 17 50194375 missense variant C/A;T snv 6
rs67394386 1.000 0.120 17 50188131 missense variant C/A;T snv 3
rs67368147 0.925 0.120 17 50191805 missense variant C/A;T snv 2
rs67445413 0.925 0.120 17 50189876 missense variant C/A;T snv 2
rs1555574303 0.790 0.240 17 50196172 missense variant C/G snv 7
rs1114167388 1.000 0.120 17 50191840 missense variant C/G snv 1
rs72645363 1.000 0.120 17 50195931 missense variant C/G snv 1
rs66490707 0.790 0.240 17 50195231 splice donor variant C/G;T snv 7
rs67693970 0.882 0.120 17 50190099 missense variant C/G;T snv 3
rs72645357 0.776 0.240 17 50196163 missense variant C/T snv 8
rs72651658 0.827 0.200 17 50190861 missense variant C/T snv 7.0E-06 5
rs72653131 0.882 0.120 17 50190045 missense variant C/T snv 3
rs72656332 0.882 0.120 17 50186895 missense variant C/T snv 3
rs768171831 0.882 0.120 7 94426011 missense variant C/T snv 1.2E-04; 4.0E-06 5.6E-05 3
rs66523073 0.925 0.120 17 50188777 missense variant C/T snv 2
rs72651645 0.925 0.160 17 50191463 missense variant C/T snv 2
rs72653178 0.925 0.120 17 50188619 missense variant C/T snv 2
rs72654795 0.925 0.120 17 50188565 missense variant C/T snv 2