Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs212389 0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 3
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs3093023 0.851 0.160 6 167120802 intron variant G/A snv 0.34 4
rs3761847 0.827 0.200 9 120927961 intron variant G/A snv 0.52 4
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 4
rs934734 0.925 0.160 2 65368452 intron variant G/A;T snv 0.54 4
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs13314993 0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs17035378 0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs13315591 0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs296547 0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs4675374 0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs4819388 0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5
rs11712165 0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 8