| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs755416212 | 1 | 97691775 | missense variant | C/T | snv | 1.2E-05 | 1 | ||||
| rs760545501 | 2 | 224359374 | regulatory region variant | C/T | snv | 1.2E-04 | 1 | ||||
| rs9644778 | 8 | 7052132 | downstream gene variant | A/C | snv | 0.34 | 1 | ||||
| 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 |