Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 9
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs1057519965 1.000 0.080 17 49619280 missense variant G/A;C snv 8.0E-06 1
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs80357382 0.763 0.240 17 43106457 missense variant T/C snv 4.0E-06 7
rs193921065 1.000 0.080 17 49619062 missense variant G/C snv 4.0E-06 1
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 20
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37