Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519371 0.925 0.200 17 37710576 frameshift variant -/G delins 2
rs886041820 1.000 0.200 17 37739577 frameshift variant -/G delins 1
rs1568645768 1.000 0.200 17 37710653 stop gained -/T delins 1
rs1568665905 1.000 0.200 17 37733730 frameshift variant -/TGTT delins 1
rs193922489 1.000 0.200 17 37739507 frameshift variant A/- del 1
rs193922486 1.000 0.200 17 37744664 stop gained A/C;T snv 1
rs193922482 1.000 0.200 17 37704931 missense variant A/G snv 7.0E-06 1
rs193922490 1.000 0.200 17 37739473 missense variant A/G snv 1
rs1555833144 1.000 0.200 17 37744764 frameshift variant C/- delins 1
rs1555830002 1.000 0.200 17 37733556 splice donor variant C/A snv 1
rs193922488 1.000 0.200 17 37739640 splice acceptor variant C/A snv 1
rs121918671 1.000 0.200 17 37744584 stop gained C/A;G snv 4.1E-06 1
rs1568670479 1.000 0.200 17 37739439 splice donor variant C/A;T snv 1
rs193922492 1.000 0.200 17 37731691 missense variant C/A;T snv 1.2E-05 1
rs529294719 1.000 0.200 17 37733611 missense variant C/G;T snv 2.4E-05 1
rs121918675 1.000 0.200 17 37739490 missense variant C/T snv 1
rs1555832998 1.000 0.200 17 37744540 splice donor variant C/T snv 1
rs1568670533 1.000 0.200 17 37739471 stop gained C/T snv 1
rs193922487 1.000 0.200 17 37744541 missense variant C/T snv 1
rs886043813 1.000 0.200 17 37731756 missense variant C/T snv 1
rs914046953 1.000 0.200 17 37731787 missense variant C/T snv 1
rs587776771 0.925 0.240 17 37744839 frameshift variant G/- delins 2
rs1568665590 1.000 0.200 17 37733577 frameshift variant G/- delins 1
rs1057517744 1.000 0.200 17 37739443 stop gained G/A snv 1
rs1057524479 1.000 0.200 17 37699168 stop gained G/A snv 1