| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs483353055 | 0.827 | 0.200 | 1 | 216200031 | missense variant | C/T | snv | 6 | |||
| rs398124619 | 0.851 | 0.200 | 1 | 215970720 | stop gained | C/A | snv | 8.0E-06 | 2.8E-05 | 5 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs483353055 | 0.827 | 0.200 | 1 | 216200031 | missense variant | C/T | snv | 6 | |||
| rs398124619 | 0.851 | 0.200 | 1 | 215970720 | stop gained | C/A | snv | 8.0E-06 | 2.8E-05 | 5 |