| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057518767 | 0.851 | 0.120 | 1 | 94098874 | missense variant | A/T | snv | 5 | |||
| rs398123339 | 0.851 | 0.120 | 1 | 94113068 | splice acceptor variant | T/C | snv | 4.0E-06 | 5 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057518767 | 0.851 | 0.120 | 1 | 94098874 | missense variant | A/T | snv | 5 | |||
| rs398123339 | 0.851 | 0.120 | 1 | 94113068 | splice acceptor variant | T/C | snv | 4.0E-06 | 5 |