| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519441 | 0.925 | 0.120 | 12 | 14683243 | missense variant | A/G | snv | 4 | |||
| rs1553370260 | 0.925 | 0.320 | 2 | 15942129 | frameshift variant | -/CGCT | delins | 4 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519441 | 0.925 | 0.120 | 12 | 14683243 | missense variant | A/G | snv | 4 | |||
| rs1553370260 | 0.925 | 0.320 | 2 | 15942129 | frameshift variant | -/CGCT | delins | 4 |