| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913412 | 0.724 | 0.280 | 3 | 41224633 | missense variant | A/C;G;T | snv | 10 | |||
| rs121913409 | 0.708 | 0.400 | 3 | 41224646 | missense variant | C/A;G;T | snv | 9 | |||
| rs398123122 | 0.925 | 0.120 | 5 | 112840063 | frameshift variant | -/T | delins | 2 | |||
| rs559510809 | 0.882 | 0.120 | 5 | 112819294 | stop gained | G/A;T | snv | 4.0E-06 | 1 |