Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4845617 0.882 0.080 1 154405422 5 prime UTR variant G/A;C snv 4
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs16899974 0.827 0.120 5 34998772 missense variant C/A snv 0.24 0.19 5
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs213045 0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs2228315 0.807 0.120 12 108624122 missense variant C/T snv 0.11 0.14 7
rs3825807 0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs7217186 0.827 0.120 17 4636097 intron variant C/T snv 0.45 5
rs1764391 0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs2066715 0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs3861950 0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs57137919 0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs5351 0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs5355 0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31