| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1554776342 | 1.000 | 9 | 128691222 | frameshift variant | ACAG/- | delins | 2 | ||||
| rs1554776938 | 1.000 | 9 | 128693805 | stop gained | CTT/- | del | 1 | ||||
| rs1554776500 | 1.000 | 9 | 128691970 | missense variant | T/G | snv | 1 | ||||
| rs1564360978 | 1.000 | 9 | 128692700 | missense variant | C/T | snv | 1 | ||||
| rs1554776933 | 1.000 | 9 | 128693794 | frameshift variant | -/TA | delins | 1 |