Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 11
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs730882026 0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17