| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1554728658 | 1.000 | 0.040 | 9 | 136509877 | missense variant | C/T | snv | 1 | |||
| rs1554728034 | 1.000 | 0.040 | 9 | 136505844 | frameshift variant | ACGAGCGT/- | delins | 1 | |||
| rs1555913337 | 1.000 | 0.040 | X | 40054273 | frameshift variant | TAGAAGTCCCAAGTGC/- | del | 1 | |||
| rs1555919960 | 1.000 | 0.040 | X | 40074947 | frameshift variant | -/GT | ins | 1 |