Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1356083197 1.000 0.040 1 224434068 missense variant C/T snv 1.5E-05 1.4E-05 2
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519921 0.763 0.240 2 177234231 missense variant T/C snv 10
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs772399455 0.851 0.080 2 15942096 missense variant G/A;C snv 4.0E-06 6
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 12
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
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
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs146795390 0.827 0.080 7 55191776 missense variant G/A snv 8.0E-06 7.0E-06 8
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36