Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs9461799 | 0.807 | 0.360 | 6 | 32721752 | downstream gene variant | T/C | snv | 0.37 | 6 | ||
rs538399 | 0.925 | 0.120 | 17 | 40454413 | intron variant | A/G | snv | 0.33 | 3 | ||
rs884000 | 0.925 | 0.120 | 2 | 205815673 | regulatory region variant | C/A | snv | 0.71 | 2 |