Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 4
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 1
rs1553622530 2 214781220 stop gained C/T snv 1
rs121913348 0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs80357522 0.776 0.280 17 43093570 frameshift variant TTTT/-;TT;TTT;TTTTT delins 7.0E-06 10
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 9
rs80356962 0.807 0.200 17 43047666 stop gained C/G;T snv 4.0E-06 7.0E-06 8
rs80356978 0.827 0.200 17 43092809 stop gained C/A;T snv 7
rs80357123 0.827 0.200 17 43057078 stop gained G/A;C;T snv 1.2E-05 7
rs80357382 0.763 0.240 17 43106457 missense variant T/C snv 4.0E-06 7
rs80357906 0.827 0.200 17 43057062 frameshift variant -/G delins 1.8E-04 7
rs80358044 0.827 0.200 17 43074330 splice donor variant C/A;G;T snv 7
rs41293465 0.851 0.200 17 43045767 stop gained G/A snv 1.2E-05 6
rs62625308 0.851 0.200 17 43091924 stop gained G/A;C snv 1.2E-05 6
rs1800747 0.882 0.200 17 43063952 splice acceptor variant C/A;G;T snv 5
rs28897696 0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 5
rs80357481 0.882 0.200 17 43094317 stop gained G/C;T snv 5
rs80357888 0.882 0.200 17 43094023 frameshift variant ATTTA/- delins 5
rs397509173 0.925 0.200 17 43104120 splice donor variant A/C;G;T snv 4
rs587781632 0.925 0.200 17 43106476 splice donor variant A/C;T snv 4
rs80356923 0.882 0.200 17 43091891 stop gained C/A;T snv 9.9E-05 4
rs80357006 0.925 0.200 17 43092274 stop gained A/C;G;T snv 1.2E-05 4
rs80357086 0.851 0.200 17 43106480 stop gained A/G;T snv 4
rs80357303 0.925 0.200 17 43071113 stop gained T/A;G snv 4.0E-06 4
rs80357310 0.925 0.200 17 43091870 stop gained C/A;G snv 4.0E-06 4