Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 118
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801200 0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 117
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 81
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 53
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs2240688 0.790 0.160 4 15968726 3 prime UTR variant T/G snv 0.22 7
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2302254 0.752 0.240 17 51153539 5 prime UTR variant C/T snv 0.22 15
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 14
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73
rs2736109 0.851 0.120 5 1296644 upstream gene variant C/T snv 0.32 4
rs2808668
XPA
0.851 0.120 9 97690153 intron variant C/G;T snv 7
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs2856836 0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26 9