| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs115025532 | 1.000 | 0.080 | 22 | 50032791 | intron variant | G/A;C | snv | 2.5E-02 | 1 | ||
| rs56330886 | 22 | 50054998 | intron variant | T/G | snv | 5.9E-02 | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs115025532 | 1.000 | 0.080 | 22 | 50032791 | intron variant | G/A;C | snv | 2.5E-02 | 1 | ||
| rs56330886 | 22 | 50054998 | intron variant | T/G | snv | 5.9E-02 | 1 |