| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs147105770 | 0.776 | 0.280 | 16 | 13935697 | missense variant | C/G;T | snv | 1.2E-05; 6.4E-05 | 5 | ||
| rs397509403 | 0.851 | 0.200 | 16 | 13928149 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs397509404 | 1.000 | 16 | 13935661 | stop gained | -/A | delins | 1 |