Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs3024490 0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs7453920 0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs2303428 0.776 0.240 2 47476361 splice region variant T/A;C;G snv 4.0E-06; 0.12 9
rs414171 0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs371194629 0.790 0.320 6 29830804 3 prime UTR variant -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT ins 8
rs737241
AFP
0.827 0.120 4 73451012 intron variant G/A;C snv 7
rs1049334 0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv 6
rs79037040 0.807 0.160 8 23225458 non coding transcript exon variant G/A;C;T snv 6
rs1054690270 0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs10853728 0.851 0.160 19 39254506 downstream gene variant C/A;G;T snv 5
rs10932029 0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs1265115 0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv 5
rs28381975 0.827 0.200 3 33798239 intron variant -/TTACGTACCTGTGCA;TTCCGTACCTGTGCA;TTTCGTACCTGTGCA delins 5
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5
rs3130779 0.925 0.080 6 30904426 upstream gene variant A/C;G;T snv 5
rs6147150 0.827 0.160 2 211380365 3 prime UTR variant -/AAAATAGGATTG delins 5
rs9268645 0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs11465817 0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs2267716 0.851 0.120 7 30677027 intron variant T/A;C snv 4
rs2723176 0.851 0.200 2 112914932 intron variant A/C;G snv 4
rs33932899 0.851 0.240 16 11254354 intron variant C/G;T snv 4
rs4656942 0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs6141 0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 4
rs9277542 0.851 0.280 6 33087470 3 prime UTR variant T/A;C snv 4