Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
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
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs174583 0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111