Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9332739 0.763 0.360 6 31936027 missense variant G/A;C snv 4.1E-06; 3.9E-02 4
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 4
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs6857 0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs641153 0.790 0.160 6 31946403 missense variant G/A;T snv 9.6E-02; 4.1E-06 4
rs1136287 0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 1
rs4151667 0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 1
rs2070895 0.807 0.120 15 58431740 intron variant G/A snv 0.33 7
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 5
rs11755724 0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 5
rs141853578
CFI
0.807 0.040 4 109764664 missense variant C/T snv 4.2E-04 3.9E-04 4
rs79037040 0.807 0.160 8 23225458 non coding transcript exon variant G/A;C;T snv 4
rs943080 0.807 0.040 6 43858890 TF binding site variant C/T snv 0.61 4
rs1329428
CFH
0.807 0.160 1 196733680 intron variant C/T snv 0.44 3
rs13278062 0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 1
rs2072633 0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 1
rs2588809 0.807 0.160 14 68193711 intron variant T/C snv 0.80 1
rs422951 0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 1
rs2740488 0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs2043085 0.827 0.080 15 58388755 intron variant T/C snv 0.54 6
rs3138141 0.827 0.040 12 55721994 3 prime UTR variant C/A snv 0.19 0.16 5