Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 5
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs11080055 0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 5
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 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
rs1831282
CFH
1.000 0.040 1 196704863 intron variant A/C snv 0.62 2