Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 1
rs1057519985 0.724 0.360 17 7673763 missense variant T/A;C;G snv 1
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 1
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 1
rs148924904 0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 1
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 1
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 1
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 1
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 1
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 1
rs371409680 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 1
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 1
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 1
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 1
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs587780076 17 7673743 missense variant C/A;T snv 8.0E-06; 8.0E-06 1
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 1
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 1
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 1
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 1