Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199971565 0.925 0.080 4 112648384 mature miRNA variant ACTT/- delins 2.1E-02 3
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs2856836 0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26 9
rs1143633 0.752 0.280 2 112832890 intron variant C/G;T snv 10
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 45
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 91
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 28
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 79
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 26
rs2515401 0.882 0.080 2 113062899 3 prime UTR variant T/A;C snv 2
rs2515402 0.925 0.080 2 113063003 3 prime UTR variant C/A snv 0.65 2
rs3180235 0.882 0.080 2 113063095 3 prime UTR variant A/G snv 0.65 2
rs2472188 0.925 0.080 2 113063237 3 prime UTR variant C/G snv 0.65 2
rs957201 0.925 0.080 2 113063623 3 prime UTR variant T/C snv 0.65 2
rs1457547311 0.851 0.080 2 113131082 synonymous variant G/A snv 4.0E-06 4
rs9005 0.851 0.160 2 113133835 3 prime UTR variant G/A snv 0.29 4
rs4353229 0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6
rs10787498 0.925 0.080 10 113729891 3 prime UTR variant T/G snv 0.38 2
rs12247479 0.925 0.080 10 113730301 3 prime UTR variant G/A snv 0.16 2
rs1127687 0.925 0.080 10 113730350 3 prime UTR variant G/A snv 0.23 2
rs9841504 0.827 0.120 3 114643917 intron variant C/G;T snv 6
rs3807987 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs7804372 0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs40239
MET
0.851 0.120 7 116677823 intron variant G/A snv 0.87 4
rs1665650 0.752 0.160 10 116727589 intron variant T/C snv 0.69 3