| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs122458138 | 1.000 | 0.080 | X | 109661643 | missense variant | G/T | snv | 1 | |||
| rs122458139 | 1.000 | 0.080 | X | 109674403 | missense variant | G/A | snv | 1 | |||
| rs1569423317 | 1.000 | 0.080 | X | 109669175 | splice acceptor variant | T/C | snv | 1 |