| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1554728034 | 1.000 | 0.040 | 9 | 136505844 | frameshift variant | ACGAGCGT/- | delins | 1 | |||
| rs1057519936 | 0.776 | 0.200 | 3 | 179234284 | missense variant | A/G;T | snv | 11 | |||
| rs1057519938 | 0.776 | 0.160 | 3 | 179203764 | missense variant | A/C;T | snv | 10 | |||
| rs1057519939 | 0.776 | 0.160 | 3 | 179203763 | missense variant | A/C | snv | 10 | |||
| rs1555919960 | 1.000 | 0.040 | X | 40074947 | frameshift variant | -/GT | ins | 1 |