| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519395 | 1.000 | 0.080 | 22 | 50721861 | frameshift variant | TG/- | delins | 2 | |||
| rs1057519406 | 1.000 | 0.080 | 22 | 50684651 | missense variant | G/T | snv | 2 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519395 | 1.000 | 0.080 | 22 | 50721861 | frameshift variant | TG/- | delins | 2 | |||
| rs1057519406 | 1.000 | 0.080 | 22 | 50684651 | missense variant | G/T | snv | 2 |