Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
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
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs9350 0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs1458974438 0.807 0.080 19 1206957 missense variant G/A snv 9
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs3213245 0.742 0.240 19 43575535 5 prime UTR variant G/A snv 0.65 0.60 13