| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1555630216 | 0.790 | 0.160 | 18 | 10714931 | splice acceptor variant | C/T | snv | 22 | |||
| rs1555648288 | 0.790 | 0.160 | 18 | 10795003 | splice acceptor variant | C/T | snv | 22 | |||
| rs1557055405 | 0.807 | 0.400 | X | 153743532 | missense variant | T/A | snv | 21 |