| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs886037774 | 0.882 | 0.120 | 8 | 19955993 | missense variant | T/C | snv | 7 | |||
| rs886037775 | 0.882 | 0.120 | 8 | 19960948 | missense variant | A/T | snv | 7 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs886037774 | 0.882 | 0.120 | 8 | 19955993 | missense variant | T/C | snv | 7 | |||
| rs886037775 | 0.882 | 0.120 | 8 | 19960948 | missense variant | A/T | snv | 7 |