Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs13119723 0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2023305 0.851 0.280 6 167111410 intron variant C/T snv 0.38 4
rs2082940 0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62