Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1057519912 0.776 0.200 X 71129408 missense variant C/G;T snv 11
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
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
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
rs2740574 0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs887303970 0.776 0.280 4 24799565 missense variant C/T snv 8.8E-06 7.0E-06 10
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4919743 0.925 0.080 12 52915800 intron variant G/A snv 0.13 5
rs755100942 0.724 0.320 13 49630894 stop gained G/A snv 4.2E-06 17