| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587784365 | 0.882 | 19 | 49861800 | frameshift variant | -/GTCGATGGCGACCCGTT | delins | 1.7E-04 | 1.8E-04 | 3 | ||
| rs786203983 | 1.000 | 19 | 49862188 | missense variant | C/A | snv | 4.2E-05 | 2 | |||
| rs786205207 | 0.925 | 19 | 49861847 | inframe deletion | GGT/- | delins | 2.1E-04 | 2 | |||
| rs886037744 | 1.000 | 19 | 49861671 | frameshift variant | -/CGGCT | ins | 1 | ||||
| rs1555810613 | 1.000 | 19 | 49861264 | frameshift variant | -/CAGTACAG | delins | 1 |