Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs5063 0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs137852912 0.776 0.120 1 55057454 missense variant G/A;C;T snv 7.2E-05 10
rs374603772 0.776 0.160 1 55058630 missense variant C/T snv 4.4E-05 2.8E-05 9
rs562556 0.827 0.280 1 55058564 missense variant G/A snv 0.86 0.83 8
rs28942111 0.807 0.120 1 55044016 missense variant T/A snv 7
rs28362261 0.851 0.160 1 55058129 missense variant A/G snv 1.2E-03 4.8E-03 6
rs564427867 0.807 0.160 1 55039931 missense variant G/A snv 2.8E-05 2.8E-05 6
rs11583680 0.882 0.200 1 55039995 missense variant C/G;T snv 1.6E-05; 0.11 3
rs141502002 0.882 0.080 1 55058549 missense variant C/T snv 6.0E-04 2.8E-03 3
rs1553135971 0.882 0.080 1 55044021 missense variant A/G snv 3
rs28362263 1.000 0.080 1 55058182 missense variant G/A;C snv 7.2E-03 3
rs752849346 0.882 0.080 1 25554000 missense variant C/T snv 3.2E-05 2.1E-05 3
rs794728683 0.882 0.080 1 55052398 missense variant G/A;T snv 4.0E-06 3
rs1057519691 0.925 0.080 1 55043958 missense variant T/C;G snv 2
rs143394031 0.925 0.080 1 55058640 missense variant G/A;C;T snv 1.6E-05; 4.9E-05; 1.6E-05 2
rs778738291 0.925 0.080 1 55044020 missense variant G/A snv 1.6E-05 7.0E-06 2
rs778849441 0.925 0.080 1 55058538 stop gained C/A;G;T snv 4.0E-06; 1.2E-05; 2.4E-05 2
rs1254346075 1.000 0.080 1 55057508 missense variant G/A;T snv 7.0E-06 1
rs1372204035 1.000 0.080 1 55039977 missense variant C/G snv 1
rs139669564 1.000 0.080 1 55058631 missense variant G/A snv 2.5E-04 9.1E-05 1
rs1553135400 1.000 0.080 1 55039913 missense variant G/A snv 1