| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1554110735 | 0.776 | 0.200 | 6 | 10398693 | frameshift variant | TT/- | delins | 13 | |||
| rs74315439 | 0.790 | 0.200 | 21 | 43172104 | missense variant | C/A;T | snv | 7 | |||
| rs1243762658 | 0.851 | 0.160 | 4 | 182754413 | missense variant | C/A;G | snv | 4.2E-06 | 7.0E-06 | 5 | |
| rs755000701 | 0.851 | 0.160 | 4 | 182799938 | missense variant | C/T | snv | 9.2E-06 | 1.4E-05 | 5 |