| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057518968 | 1.000 | 0.040 | 18 | 34794065 | missense variant | A/G | snv | 8.0E-06 | 2.1E-05 | 2 | |
| rs397516996 | 1.000 | 0.080 | 12 | 32896718 | frameshift variant | C/- | delins | 2 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057518968 | 1.000 | 0.040 | 18 | 34794065 | missense variant | A/G | snv | 8.0E-06 | 2.1E-05 | 2 | |
| rs397516996 | 1.000 | 0.080 | 12 | 32896718 | frameshift variant | C/- | delins | 2 |