| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs143137713 | 0.925 | 3 | 148996462 | missense variant | G/C | snv | 1.0E-03 | 1.1E-03 | 3 | ||
| rs1559834349 | 0.925 | 3 | 148996312 | stop gained | G/T | snv | 2 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs143137713 | 0.925 | 3 | 148996462 | missense variant | G/C | snv | 1.0E-03 | 1.1E-03 | 3 | ||
| rs1559834349 | 0.925 | 3 | 148996312 | stop gained | G/T | snv | 2 |