Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
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
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs41423247 0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs2229094 0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 17
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs2606345 0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs6198 0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs9470080 0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs368939818 0.763 0.280 11 49156734 missense variant G/A snv 4.0E-05 2.1E-05 13
rs755001634 0.763 0.280 11 49154384 stop gained G/A snv 1.2E-05 13
rs6994992 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13