Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98