Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
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
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs10814325 0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11662595 0.882 0.120 18 24477006 missense variant A/G snv 8.6E-02 7.6E-02 7
rs11788747 0.851 0.240 9 36105267 synonymous variant A/C;G snv 4.0E-06; 0.34 6
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913444 0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96