Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2180314 0.776 0.200 6 52752933 missense variant C/G snv 0.60 0.52 8
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
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
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs3760396 0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15 13