Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2793094 0.925 0.080 1 231741236 intron variant G/A snv 0.97 3
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs174697 0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs242939 0.882 0.120 17 45818213 intron variant C/T snv 0.86 3
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs1488864 0.851 0.080 11 6321099 intron variant T/G snv 0.80 4
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs738499 0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs7997012 0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs4580704 0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs3096140 0.882 0.080 5 37832731 intron variant G/A snv 0.69 5
rs386231 0.882 0.080 1 162356033 intron variant C/T snv 0.68 4
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs10410544 0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs3758391 0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs242941 0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs11824092 0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs2412646 0.882 0.120 4 55452605 3 prime UTR variant T/C snv 0.58 3
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92