| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121918683 | 1.000 | 0.160 | 8 | 127738519 | missense variant | A/C | snv | 2 | |||
| rs28933407 | 1.000 | 0.160 | 8 | 127738431 | missense variant | C/T | snv | 2 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121918683 | 1.000 | 0.160 | 8 | 127738519 | missense variant | A/C | snv | 2 | |||
| rs28933407 | 1.000 | 0.160 | 8 | 127738431 | missense variant | C/T | snv | 2 |