Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs372043866 0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs121913369 0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs3743073 0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1458974438 0.807 0.080 19 1206957 missense variant G/A snv 9
rs588765 0.827 0.200 15 78573083 intron variant T/A;C snv 6
rs772399455 0.851 0.080 2 15942096 missense variant G/A;C snv 4.0E-06 6
rs775514340 0.882 0.080 6 53041202 missense variant T/A;C snv 4.0E-06 5
rs1256061 14 64236875 intron variant G/A;T snv 5