Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2144908 0.851 0.120 20 44357077 intron variant G/A snv 0.18 5
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs1862513 0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs773641005 0.742 0.240 16 58723829 missense variant T/C snv 14
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs2229616 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36