Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 23
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 9
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 8
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 7
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 5
rs57942103 1.000 0.040 8 105501233 intron variant A/C snv 0.25 3