Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs7528419 0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 4
rs2144300 0.882 0.040 1 230159169 intron variant C/T snv 0.44 4
rs4537545 0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs611917 1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32 4
rs17114036 0.851 0.120 1 56497149 intron variant A/G snv 0.11 3
rs1748195 0.851 0.120 1 62583922 intron variant C/G;T snv 3
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs2281719 1.000 0.040 1 230161913 intron variant C/T snv 0.45 3
rs4845625 0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 3
rs6698843 0.925 0.080 1 109264212 synonymous variant C/A;T snv 4.0E-06; 0.44 3
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 1
rs1150256 0.925 0.120 1 206899788 intron variant G/A snv 0.40 1
rs12566888 0.807 0.280 1 156899255 intron variant G/T snv 0.26 1
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 1
rs17114046 0.925 0.040 1 56500678 intron variant A/G snv 0.12 1