| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909749 | 1.000 | 4 | 157143807 | missense variant | G/A | snv | 2 | ||||
| rs281864922 | 1.000 | 4 | 157136891 | splice region variant | G/A | snv | 4.8E-05 | 3.5E-05 | 2 | ||
| rs1415892964 | 1.000 | 4 | 157120554 | splice acceptor variant | A/G | snv | 1 | ||||
| rs1560962569 | 1.000 | 4 | 157136613 | frameshift variant | -/A | delins | 1 | ||||
| rs1560962636 | 1.000 | 4 | 157136641 | frameshift variant | C/- | delins | 1 | ||||
| rs398122856 | 1.000 | 4 | 157136872 | missense variant | T/G | snv | 1 |