| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912745 | 0.807 | 0.200 | 17 | 44255708 | missense variant | G/A;T | snv | 9 | |||
| rs121912756 | 17 | 44257538 | missense variant | C/T | snv | 8.0E-06 | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912745 | 0.807 | 0.200 | 17 | 44255708 | missense variant | G/A;T | snv | 9 | |||
| rs121912756 | 17 | 44257538 | missense variant | C/T | snv | 8.0E-06 | 1 |