| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs118192250 | 0.851 | 0.120 | 8 | 132175457 | missense variant | C/A | snv | 1 | |||
| rs1569315842 | 1.000 | 0.080 | X | 100408107 | frameshift variant | -/G | delins | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs118192250 | 0.851 | 0.120 | 8 | 132175457 | missense variant | C/A | snv | 1 | |||
| rs1569315842 | 1.000 | 0.080 | X | 100408107 | frameshift variant | -/G | delins | 1 |