| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs569681869 | 0.925 | 0.040 | 2 | 227059468 | missense variant | C/G | snv | 7.2E-05 | 3.5E-05 | 6 | |
| rs533297350 | 1.000 | 0.040 | 2 | 227010441 | missense variant | C/T | snv | 7.2E-05 | 3.5E-05 | 5 | |
| rs1556411578 | X | 108595507 | coding sequence variant | AAGGTGACA/- | delins | 4 | |||||
| rs1556463583 | X | 108695350 | frameshift variant | -/A | delins | 2 | |||||
| rs779593707 | 1 | 16049884 | stop gained | -/AATA | delins | 1.2E-05 | 7.0E-06 | 2 |