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
rs112852289 1.000 0.080 11 61008833 frameshift variant -/T ins 5.1E-06; 5.1E-06 1
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs11352835 1.000 0.080 12 112931911 frameshift variant A/- del 0.74 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs6568431 0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs3129871 0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs12948909 0.925 0.120 17 42418584 intron variant A/C snv 0.24 3
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3
rs437179 0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs6017342 0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 3
rs630379 0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs9270986 0.882 0.160 6 32606283 intergenic variant A/C snv 0.85 3
rs9891119 0.882 0.120 17 42355962 intron variant A/C snv 0.36 3
rs17519972 1.000 0.080 1 92362948 intron variant A/C snv 0.15 2
rs17758761 1.000 0.080 17 55977164 intron variant A/C snv 4.1E-02 2
rs2524095 0.925 0.160 6 31298340 intron variant A/C snv 0.65 2
rs4807569 0.925 0.120 19 1123379 intron variant A/C snv 0.25 2
rs4948088 0.925 0.160 7 50959497 intron variant A/C snv 0.96 2
rs12599600 1.000 0.080 16 11340245 intron variant A/C snv 0.75 1
rs1458175 1.000 0.080 12 41572059 intron variant A/C snv 0.59 1
rs1611715 1.000 0.080 6 29861705 intron variant A/C snv 0.30 1
rs2726518 1.000 0.080 4 105252042 intron variant A/C snv 0.63 1