Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2082412 0.925 0.120 5 159290781 downstream gene variant G/A snv 0.27 2
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs2546890 0.882 0.200 5 159332892 non coding transcript exon variant A/G snv 0.52 3
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs30187 0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs71624119 0.776 0.200 5 56144903 intron variant G/A snv 0.17 8
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2301436 0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs610604 0.827 0.240 6 137878280 intron variant G/T snv 0.58 5
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223