| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121917772 | 0.882 | 0.240 | 16 | 20348298 | missense variant | A/C | snv | 3 | |||
| rs121917773 | 1.000 | 0.120 | 16 | 20348253 | missense variant | A/G | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121917772 | 0.882 | 0.240 | 16 | 20348298 | missense variant | A/C | snv | 3 | |||
| rs121917773 | 1.000 | 0.120 | 16 | 20348253 | missense variant | A/G | snv | 1 |