| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121918136 | 1.000 | 3 | 49022146 | start lost | T/C;G | snv | 8.5E-06 | 1 | |||
| rs121918134 | 1.000 | 3 | 49022497 | missense variant | G/A;C | snv | 4.0E-06 | 1 | |||
| rs121918135 | 1.000 | 3 | 49022903 | missense variant | G/C | snv | 1 |