| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387906625 | 1.000 | 15 | 48463219 | missense variant | T/C | snv | 1 | ||||
| rs1566911957 | 0.776 | 0.200 | 15 | 48496204 | frameshift variant | GTACACATTCA/- | delins | 8 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387906625 | 1.000 | 15 | 48463219 | missense variant | T/C | snv | 1 | ||||
| rs1566911957 | 0.776 | 0.200 | 15 | 48496204 | frameshift variant | GTACACATTCA/- | delins | 8 |