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 |