Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs2288904 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
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
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs9943582 0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs4845625 0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs7173743 0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24