| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61752138 | 0.882 | 0.120 | 12 | 7209700 | missense variant | T/G | snv | 3 | |||
| rs1565673352 | 1.000 | 0.080 | 12 | 7191613 | stop gained | G/T | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61752138 | 0.882 | 0.120 | 12 | 7209700 | missense variant | T/G | snv | 3 | |||
| rs1565673352 | 1.000 | 0.080 | 12 | 7191613 | stop gained | G/T | snv | 1 |