Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12733285 0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs3734254 0.752 0.240 6 35427233 3 prime UTR variant C/T snv 0.69 14
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
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
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs1864169 0.851 0.200 14 81203689 intron variant G/T snv 0.78 5
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1342387 0.776 0.120 1 202945228 intron variant T/C snv 0.53 12