| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908569 | 1.000 | 0.200 | 2 | 88583430 | missense variant | C/T | snv | 1 | |||
| rs121908570 | 1.000 | 0.200 | 2 | 88590826 | stop gained | C/A;G | snv | 1.2E-05 | 1 | ||
| rs1558652941 | 1.000 | 0.200 | 2 | 88585918 | frameshift variant | TTTC/- | delins | 1 | |||
| rs797045558 | 1.000 | 0.200 | 2 | 88585926 | frameshift variant | AC/- | delins | 1 | |||
| rs864621972 | 1.000 | 0.200 | 2 | 88588875 | stop gained | G/A | snv | 1 | |||
| rs869025178 | 1.000 | 0.200 | 2 | 88590572 | frameshift variant | -/A | delins | 1 | |||
| rs1553407942 | 1.000 | 0.200 | 2 | 88574725 | stop gained | G/A | snv | 1 | |||
| rs869025179 | 1.000 | 0.200 | 2 | 88570873 | splice donor variant | C/T | snv | 1 |