Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 3
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs2205960 0.763 0.400 1 173222336 intergenic variant G/A;T snv 2
rs3024493 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 2
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 2
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 2
rs704840 0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 2
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs1012507 1.000 0.080 1 173250332 intergenic variant G/T snv 0.32 1
rs10489265 0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs10798269 1.000 0.080 1 173340574 intergenic variant A/G;T snv 1
rs10889681 0.925 0.160 1 67333487 intron variant T/A;C snv 1
rs10911628 1.000 0.080 1 184680369 intergenic variant C/A snv 9.4E-02 1
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 1
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 1
rs12068671 0.925 0.160 1 172711891 intergenic variant T/C snv 0.23 1
rs1518111 0.790 0.360 1 206771300 intron variant T/C snv 0.71 1
rs16840639 0.925 0.120 1 196855643 intron variant T/C snv 0.23 1
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1