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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs2779248 0.882 0.160 17 27800806 intron variant T/C snv 0.39 4
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1532624 0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs7222331 0.925 0.120 17 40995605 upstream gene variant C/T snv 0.24 3
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1137933 0.882 0.160 17 27778906 synonymous variant G/A snv 0.20 0.21 4
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs290487 0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs11771443 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169