| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs672601334 | 0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv | 18 | |||
| rs1555741826 | 0.776 | 0.280 | 19 | 49601646 | frameshift variant | TGCC/- | delins | 16 | |||
| rs730881014 | 0.776 | 0.360 | 1 | 155904494 | stop gained | A/C;G;T | snv | 15 | |||
| rs869025191 | 0.827 | 0.160 | 1 | 155904739 | missense variant | C/A;G;T | snv | 9 |