Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 45
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 31
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 29
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 27
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 26
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs9350 0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 13
rs1553260624 0.763 0.080 1 226064454 missense variant G/A snv 13
rs172378 0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs2536 0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 11
rs3790843 0.827 0.160 1 200041696 intron variant C/T snv 0.29 7
rs4149963 0.851 0.120 1 241872080 missense variant C/T snv 0.11; 6.8E-05 7.6E-02 7
rs6691378 0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19 6
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 6
rs768827923 0.851 0.080 1 9721816 missense variant T/G snv 6