| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607168 | 1.000 | 1 | 160425122 | missense variant | T/C | snv | 1 | ||||
| rs267607167 | 1.000 | 1 | 160421171 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607168 | 1.000 | 1 | 160425122 | missense variant | T/C | snv | 1 | ||||
| rs267607167 | 1.000 | 1 | 160421171 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 |