Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs121913503 0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 9
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs2071286 0.752 0.280 6 32212119 intron variant C/T snv 0.17 12
rs2274084 0.882 0.240 13 20189503 missense variant C/T snv 5.4E-02 2.2E-02 6
rs138228187 0.925 0.120 11 126292650 missense variant C/T snv 4.0E-05 1.4E-05 3
rs61756766 0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs10190751 0.882 0.120 2 201141373 splice acceptor variant G/A snv 0.18 0.26 4
rs1351687973 0.925 0.120 1 3731497 missense variant G/A snv 1.6E-05 3
rs535311760 0.925 0.120 1 3730979 missense variant G/A snv 1.2E-05; 8.2E-06 3
rs867329357 0.925 0.120 13 102872275 missense variant G/A snv 4.0E-06 4.9E-05 3
rs8177400 0.882 0.160 11 126292695 missense variant G/A;C;T snv 2.8E-03; 1.2E-05 4
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs867830180 0.925 0.120 20 63695147 missense variant G/A;T snv 3
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1057519833 0.925 0.120 7 148809375 missense variant G/C snv 3
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs2466571 0.925 0.120 1 207766701 intron variant G/T snv 0.46 3
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs6676671 0.882 0.160 1 206779403 intron variant T/A snv 0.32 4
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134