Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs925489 0.882 0.080 9 97784318 intron variant C/T snv 0.71 5
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 3
rs11175834 0.925 0.080 12 65598856 intron variant C/T snv 0.14 2
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 2
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 2
rs949963 0.925 0.160 2 102153326 intron variant C/T snv 0.22 2
rs2107538 0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27 1
rs2516839 0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 1
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs1057519855 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 1
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 4
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs2622590 0.925 0.080 8 55445714 intron variant G/A snv 0.15 3
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 2
rs1874564 0.925 0.080 4 76936952 intergenic variant G/A snv 0.58 2
rs9858271 0.925 0.080 3 59559604 intron variant G/A snv 0.80 2
rs3737787 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 1
rs537209983 0.882 0.080 14 36517378 missense variant G/A snv 1.7E-04 8.4E-05 1
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs121913375 0.851 0.240 7 140753339 missense variant G/A;C snv 5
rs28937584 0.925 0.080 14 81143955 missense variant G/A;C snv 4.0E-06 1
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 14
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 10
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 3