Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs2298566 0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 5
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs2277680 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 10
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs3900940 0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38