Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57137919 0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs1136287 0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 8
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs641153 0.790 0.160 6 31946403 missense variant G/A;T snv 9.6E-02; 4.1E-06 7
rs1064039 0.827 0.200 20 23637790 missense variant C/G;T snv 0.20 6
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs1142 0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs141853578
CFI
0.807 0.040 4 109764664 missense variant C/T snv 4.2E-04 3.9E-04 6
rs147859257
C3
0.827 0.040 19 6718135 missense variant T/G snv 2.8E-03 2.4E-03 6
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 6
rs79037040 0.807 0.160 8 23225458 non coding transcript exon variant G/A;C;T snv 6
rs943080 0.807 0.040 6 43858890 TF binding site variant C/T snv 0.61 6
rs11080055 0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs114254831 0.827 0.040 6 32187804 intron variant A/G snv 5
rs116503776 0.827 0.040 6 31962685 intron variant G/A snv 5
rs13095226 0.851 0.040 3 99677428 intron variant T/C snv 9.5E-02 5
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 5
rs3138141 0.827 0.040 12 55721994 3 prime UTR variant C/A snv 0.19 0.16 5
rs61941274 0.827 0.160 12 111694806 intron variant G/A;T snv 5
rs62358361
C9
0.851 0.040 5 39327786 intron variant G/C;T snv 5
rs72802342 0.851 0.040 16 75200974 downstream gene variant C/A snv 6.2E-02 5
rs73036519 0.851 0.040 19 45245104 intron variant G/A;C snv 5
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs11884770 0.851 0.040 2 227222204 intron variant T/A;C snv 4