| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894928 | 0.882 | 0.040 | X | 18647303 | missense variant | C/G;T | snv | 1.1E-05 | 3 | ||
| rs104894930 | 0.882 | 0.040 | X | 18642071 | missense variant | G/A | snv | 3 | |||
| rs281865365 | 0.882 | 0.040 | X | 18642042 | missense variant | G/A;T | snv | 3 | |||
| rs61752144 | 0.882 | 0.040 | X | 18644616 | missense variant | C/A;G | snv | 3 |