Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs1048709 0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs4505848 0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs4788084 0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs10863888 0.851 0.280 1 211329427 intron variant A/C;G;T snv 4