Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9517723 0.925 0.200 13 99432425 non coding transcript exon variant T/C snv 0.65 2
rs10236188 1.000 0.200 7 150548168 intergenic variant T/C snv 0.49 1
rs10256482 1.000 0.200 7 150653887 intergenic variant T/C snv 0.47 1
rs112130712 1.000 0.200 18 20967783 missense variant T/C snv 1
rs1462891 1.000 0.200 8 31973417 intron variant T/C snv 0.72 1
rs2617170 1.000 0.200 12 10408358 missense variant T/C snv 0.63 0.61 1
rs5745908 1.000 0.200 15 75349341 splice donor variant T/C snv 7.2E-03 6.9E-03 1
rs755659290 1.000 0.200 16 3249480 missense variant T/C snv 1.2E-05 1.4E-05 1
rs7854303 1.000 0.200 9 5557672 missense variant T/C snv 1.00 1.00 1
rs9260997 1.000 0.200 6 29995539 upstream gene variant T/C snv 0.90 1
rs9368678 1.000 0.200 6 31304686 intron variant T/C snv 9.2E-02 1
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs1065407 1.000 0.200 5 96776379 3 prime UTR variant T/A;G snv 3.3E-05; 0.26 1
rs3789604 0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs30187 0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs104895094 0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 5
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 5
rs752637 0.925 0.280 7 128939366 intron variant T/A;C snv 2
rs10277380 1.000 0.200 7 150533604 intergenic variant T/A;C snv 1
rs2234237 0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 9
rs9517668 1.000 0.200 13 99271586 intron variant T/A snv 0.80 1
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34