| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs397518483 | 0.851 | 0.120 | 3 | 25596428 | missense variant | C/A;T | snv | 9 | |||
| rs869025222 | 0.827 | 0.240 | 3 | 25580574 | missense variant | T/C | snv | 9 | |||
| rs869025221 | 0.925 | 0.080 | 3 | 25593603 | missense variant | G/C | snv | 5 | |||
| rs397518481 | 0.925 | 0.120 | 3 | 25501230 | stop gained | C/G;T | snv | 2 | |||
| rs1553637470 | 1.000 | 3 | 25593588 | missense variant | A/T | snv | 1 | ||||
| rs397518482 | 1.000 | 3 | 25596470 | frameshift variant | -/TC | delins | 1 |