Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs213045 0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs5351 0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4845617 0.882 0.080 1 154405422 5 prime UTR variant G/A;C snv 4
rs5918 0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41