Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1013345784 1.000 0.120 17 42536274 start lost T/C;G snv 1
rs104894590 0.925 0.120 17 42544027 missense variant G/A;T snv 1.6E-05 2
rs104894591 0.925 0.120 17 42543882 stop gained C/G;T snv 4.4E-06; 2.2E-05 2
rs104894592 0.925 0.160 17 42541074 stop gained C/T snv 5.6E-05 9.8E-05 2
rs104894593 1.000 0.120 17 42543934 missense variant G/A snv 1
rs104894594 1.000 0.120 17 42543933 missense variant C/A;T snv 4.2E-06 1
rs104894595 1.000 0.120 17 42543568 missense variant C/T snv 2.0E-05 2.1E-05 1
rs104894596 1.000 0.120 17 42543450 missense variant C/A;T snv 2.7E-05 1.4E-05 1
rs104894597 1.000 0.120 17 42543699 missense variant C/T snv 3.2E-05 3.5E-05 1
rs104894598 0.882 0.160 17 42543700 missense variant G/A;C;T snv 4.4E-05; 1.2E-05 3
rs104894599 0.925 0.120 17 42536416 missense variant C/A;G;T snv 7.1E-06 2
rs104894600 1.000 0.120 17 42541125 missense variant T/C snv 1
rs104894601 1.000 0.120 17 42538691 missense variant C/T snv 3.2E-05 7.0E-06 1
rs1052471595 1.000 0.120 17 42541119 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1180591588 1.000 0.120 17 42543068 frameshift variant C/- delins 1
rs118204024 0.925 0.120 17 42536414 missense variant T/C snv 2
rs118204025 1.000 0.120 17 42541127 missense variant C/G snv 8.0E-06 1
rs1183634153 1.000 0.120 17 42543360 missense variant G/A snv 1.2E-05 1
rs1195831432 1.000 0.120 17 42544068 stop gained C/G;T snv 4.0E-06 1
rs1244655820 0.925 0.120 17 42543603 stop gained C/T snv 7.0E-06 2
rs1250949842 1.000 0.120 17 42543431 frameshift variant G/- del 4.5E-06 1
rs1276484671 1.000 0.120 17 42536507 missense variant G/A snv 2.8E-05 1
rs1305299665 1.000 0.120 17 42541111 missense variant A/G;T snv 4.0E-06 1
rs1358994052 1.000 0.120 17 42541059 missense variant G/A;C snv 1.2E-05 1
rs138387856 1.000 0.120 17 42543396 stop gained C/T snv 1.3E-05 7.0E-06 1