Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121913365 0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs397507484 0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs149680468 0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 17
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs1057520010 0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20