| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs886039469 | 0.701 | 0.560 | 10 | 76891709 | missense variant | T/C | snv | 35 | |||
| rs1563595095 | 0.776 | 0.320 | 8 | 60781285 | frameshift variant | AA/T | delins | 10 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs886039469 | 0.701 | 0.560 | 10 | 76891709 | missense variant | T/C | snv | 35 | |||
| rs1563595095 | 0.776 | 0.320 | 8 | 60781285 | frameshift variant | AA/T | delins | 10 |