| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1206165503 | 0.925 | 0.160 | 17 | 7675175 | stop gained | C/T | snv | 2 | |||
| rs1456725200 | 1.000 | 0.040 | 2 | 25246661 | missense variant | C/A;T | snv | 1 | |||
| rs758881009 | 1.000 | 0.040 | 2 | 25247628 | missense variant | C/A;T | snv | 8.0E-06; 2.4E-05 | 1 | ||
| rs587776885 | 1.000 | 0.040 | 12 | 111418745 | frameshift variant | GCGCT/- | delins | 1 |