Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140