| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854534 | 1.000 | 0.120 | 20 | 58909715 | missense variant | C/G | snv | 1 | |||
| rs137854531 | 1.000 | 0.120 | 20 | 58903569 | missense variant | T/C | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854534 | 1.000 | 0.120 | 20 | 58909715 | missense variant | C/G | snv | 1 | |||
| rs137854531 | 1.000 | 0.120 | 20 | 58903569 | missense variant | T/C | snv | 1 |