| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs779372373 | 1.000 | 0.080 | 5 | 157244381 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs121908191 | 1.000 | 5 | 157241663 | missense variant | C/T | snv | 1 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs779372373 | 1.000 | 0.080 | 5 | 157244381 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs121908191 | 1.000 | 5 | 157241663 | missense variant | C/T | snv | 1 |