Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs751141 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs688 0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs1063537 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 6
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs34713741 0.882 0.280 15 101277671 upstream gene variant C/A;T snv 0.24 3
rs852426 0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 5