Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 100
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
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 69
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 32
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 131
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
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 97
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
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 48
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4754 0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs20551 0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 110
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 11