| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80338758 | 0.790 | 0.400 | X | 71127367 | missense variant | C/A;T | snv | 9 | |||
| rs765417606 | 0.882 | 0.400 | X | 71124263 | missense variant | A/G | snv | 2.8E-05 | 8.6E-05 | 3 | |
| rs387907360 | 1.000 | 0.280 | X | 71128686 | missense variant | G/A;T | snv | 1 | |||
| rs387907361 | 1.000 | 0.280 | X | 71129131 | missense variant | T/C | snv | 1 | |||
| rs387907362 | 1.000 | 0.280 | X | 71136440 | missense variant | C/A | snv | 1 |