Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 1
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 1
rs867262025 0.790 0.360 3 179221146 missense variant G/A snv 1
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 1
rs121909237 1.000 0.040 10 87933121 missense variant C/G snv 1
rs377767347 0.742 0.520 18 51065549 missense variant G/A;C;T snv 1
rs80338963 0.776 0.280 18 51065548 missense variant C/A;G;T snv 1
rs201613442 1.000 0.040 1 74540276 missense variant G/A snv 4.0E-06 1
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
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 1
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 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
rs397514495 0.882 0.120 17 7675070 missense variant C/A;T snv 1.2E-05 1