| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs672601334 | 0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv | 18 | |||
| rs483352822 | 0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv | 16 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs672601334 | 0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv | 18 | |||
| rs483352822 | 0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv | 16 |