| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs879255280 | 0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv | 22 | |||
| rs121918347 | 0.851 | 0.080 | 7 | 129210500 | missense variant | G/T | snv | 4 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs879255280 | 0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv | 22 | |||
| rs121918347 | 0.851 | 0.080 | 7 | 129210500 | missense variant | G/T | snv | 4 |