Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913293 0.732 0.360 10 87952142 missense variant C/A;T snv 18
rs1555565492 0.776 0.160 17 17795417 frameshift variant -/G delins 18
rs587776667 0.742 0.280 10 87931090 splice donor variant G/A;C;T snv 14
rs386834070 0.851 0.360 8 99134644 stop gained C/T snv 9
rs1085308045 0.807 0.160 10 87933128 missense variant C/G;T snv 8
rs1085308056 0.851 0.160 10 87957850 splice region variant C/G snv 8
rs1114167293 0.807 0.320 12 6944474 splice acceptor variant A/G snv 4.0E-06 7
rs730882197 0.925 0.040 12 4525342 frameshift variant -/GTTT delins 4
rs140630794 0.925 0.040 21 36397429 missense variant A/C;G snv 1.3E-05; 4.2E-06 3