Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 10
rs209489 0.790 0.080 6 53312880 intron variant C/A snv 0.92 9
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs7549819 0.925 0.080 1 1165623 upstream gene variant C/T snv 0.88 2
rs7229639 0.763 0.080 18 48924606 intron variant A/G snv 0.87 13
rs2970847 0.882 0.200 4 23814301 synonymous variant T/C snv 0.84 0.86 3
rs180040 0.882 0.120 15 97027933 intergenic variant T/C snv 0.85 3
rs2738783 0.763 0.160 20 63677259 intron variant T/G snv 0.85 11
rs6785358 0.882 0.200 3 30602723 upstream gene variant G/A snv 0.84 4
rs7959129 1.000 0.080 12 50775325 intron variant T/G snv 0.84 3
rs4574118 1.000 0.080 2 106331987 intergenic variant C/G snv 0.84 1
rs10849432 0.790 0.080 12 6276561 intergenic variant C/T snv 0.84 9
rs928883 0.882 0.160 21 25571713 intron variant A/G snv 0.83 3
rs1051690 0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 4
rs2749812 1.000 0.080 20 23082290 3 prime UTR variant A/G snv 0.83 1
rs1950902 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs4378954 0.790 0.080 3 115931601 intron variant T/C snv 0.83 10
rs790056 0.925 0.080 1 160999795 intron variant C/T snv 0.81 0.83 2
rs2077218 1.000 0.080 10 94311804 intron variant G/A snv 0.81 1
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs7248637 1.000 0.080 19 7742141 3 prime UTR variant A/G snv 0.81 1
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs3757441 0.752 0.200 7 148827660 intron variant C/T snv 0.80 12