Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5844572 0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs104895271 0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs1310182 0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs179008 0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs1059702 0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs13119723 0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs6478109 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs743777 0.827 0.200 22 37155567 intron variant A/G snv 0.36 7
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs864537 0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1036199 0.925 0.160 5 157104725 missense variant C/A snv 0.87 0.83 3
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23