Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7447815 1.000 0.080 5 1240642 stop gained C/G;T snv 0.36; 7.6E-05 2
rs9925481 0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11739136 0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs12487736 1.000 0.080 3 47418189 missense variant C/T snv 0.54 0.47 2
rs1462059537 0.882 0.160 4 147535944 missense variant C/T snv 8.0E-06 4
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2108622 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs2149954 0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs2890565 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs3742264 0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35 17
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs771676129 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs999947969 0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12
rs1012841819 0.882 0.160 2 96115728 missense variant G/A snv 4.0E-06 4
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63