| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs764254189 | 1.000 | 18 | 12340230 | missense variant | T/C;G | snv | 5.6E-05 | 1 | |||
| rs387906889 | 1.000 | 18 | 12340334 | missense variant | T/A;C | snv | 8.0E-06 | 1 | |||
| rs727502823 | 1.000 | 18 | 12340306 | missense variant | C/T | snv | 4.0E-06 | 1 |