| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs752171066 | 0.882 | 0.080 | 17 | 8174573 | inframe deletion | AAG/- | delins | 2.0E-05 | 2.1E-05 | 3 | |
| rs1555526172 | 1.000 | 17 | 8175980 | missense variant | T/C | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs752171066 | 0.882 | 0.080 | 17 | 8174573 | inframe deletion | AAG/- | delins | 2.0E-05 | 2.1E-05 | 3 | |
| rs1555526172 | 1.000 | 17 | 8175980 | missense variant | T/C | snv | 1 |