Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1169305 1.000 0.040 12 120999579 missense variant A/G snv 1.00 0.99 2
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs5128 0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8
rs767870 0.882 0.120 12 1780657 intron variant G/A;C snv 0.82 4
rs4149117 0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs11574
ID3
1.000 0.040 1 23559007 missense variant T/A;C snv 0.80 2
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
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
rs222747 0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801262 0.882 0.120 2 181678728 missense variant T/C snv 0.70 0.68 4
rs3736544 0.882 0.160 4 55443825 synonymous variant A/G snv 0.70 0.69 4
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs4918 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs10010131 0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs5435 0.851 0.200 17 7283804 missense variant T/A;C snv 0.65 6
rs4606565 1.000 0.040 12 124954003 splice region variant A/G snv 0.65 0.57 2
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25