| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs864309532 | 0.807 | 0.360 | X | 134393952 | missense variant | G/A | snv | 7 | |||
| rs132630297 | 0.925 | 0.280 | X | 134425256 | stop gained | C/A;T | snv | 6 | |||
| rs104894917 | 1.000 | 0.200 | X | 134413937 | missense variant | A/G | snv | 1 | |||
| rs104894918 | 1.000 | 0.200 | X | 134413923 | missense variant | A/G | snv | 1 | |||
| rs104894919 | 1.000 | 0.200 | X | 134415055 | missense variant | A/G | snv | 1 | |||
| rs1114167289 | 1.000 | 0.200 | X | 134393515 | stop gained | C/A | snv | 1 | |||
| rs132630298 | 1.000 | 0.200 | X | 134393556 | missense variant | G/T | snv | 1 | |||
| rs132630299 | 1.000 | 0.200 | X | 134377751 | missense variant | G/A | snv | 1 | |||
| rs132630300 | 1.000 | 0.200 | X | 134377619 | start lost | T/C | snv | 1 | |||
| rs132630301 | 1.000 | 0.200 | X | 134377639 | stop gained | A/T | snv | 1 | |||
| rs1556013203 | 1.000 | 0.200 | X | 134377644 | frameshift variant | -/GG | delins | 1 | |||
| rs1556018932 | 1.000 | 0.200 | X | 134413910 | stop gained | C/T | snv | 1 | |||
| rs1556019105 | 1.000 | 0.200 | X | 134415043 | inframe deletion | ACA/- | delins | 1 | |||
| rs1569334260 | 1.000 | 0.200 | X | 134377682 | stop gained | C/A | snv | 1 | |||
| rs587777489 | 1.000 | 0.200 | X | 134417248 | missense variant | G/T | snv | 1 |