| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519019 | 1.000 | 15 | 100573936 | missense variant | C/T | snv | 1 | ||||
| rs149644940 | 1.000 | 15 | 100573695 | stop gained | A/C | snv | 1.2E-05 | 1.4E-05 | 1 | ||
| rs587777225 | 1.000 | 15 | 100573885 | frameshift variant | CATG/- | del | 1 | ||||
| rs587777226 | 1.000 | 15 | 100573650 | splice donor variant | CTTTC/- | delins | 1 |