| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121917736 | 0.851 | 0.200 | 16 | 79599013 | missense variant | T/C | snv | 4 | |||
| rs786205221 | 0.851 | 0.200 | 16 | 79599008 | missense variant | G/T | snv | 4 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121917736 | 0.851 | 0.200 | 16 | 79599013 | missense variant | T/C | snv | 4 | |||
| rs786205221 | 0.851 | 0.200 | 16 | 79599008 | missense variant | G/T | snv | 4 |