Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs7178239 1.000 0.040 15 101267907 downstream gene variant C/G snv 0.37 2
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs4149570 0.752 0.360 12 6342424 upstream gene variant A/C;G;T snv 11
rs10004195 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs28665122 0.807 0.240 15 101277522 upstream gene variant C/T snv 0.24 7
rs4794067 0.807 0.280 17 47731462 upstream gene variant T/A;C snv 0.25 7
rs17250932 0.851 0.160 17 47731941 upstream gene variant T/C snv 0.16 5
rs57348955 0.882 0.120 16 31174561 upstream gene variant G/A;C snv 3
rs6543116 0.882 0.120 2 102311266 upstream gene variant A/G snv 0.76 3
rs2227478 0.925 0.040 12 68254842 upstream gene variant A/G snv 0.37 2
rs2569192 0.925 0.120 5 140635623 upstream gene variant G/C snv 0.27 2
rs3753348 0.925 0.080 1 1208277 upstream gene variant C/G;T snv 2
rs12507813 1.000 0.040 4 165013422 upstream gene variant G/A;C;T snv 1
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1085308054 0.827 0.160 10 87952231 frameshift variant AT/- delins 7
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1053005 0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs2270450 0.827 0.200 6 46677138 3 prime UTR variant C/T snv 0.29 5
rs2563298 0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26 4
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs78645479 0.851 0.120 1 63322631 5 prime UTR variant C/G;T snv 4