| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607227 | 0.925 | 0.160 | 16 | 84154748 | missense variant | T/C;G | snv | 3 | |||
| rs267607225 | 1.000 | 0.120 | 16 | 84159744 | stop gained | C/T | snv | 1.6E-05 | 2 | ||
| rs397515339 | 0.925 | 0.160 | 16 | 84170172 | frameshift variant | -/C | delins | 2 | |||
| rs786205052 | 1.000 | 0.120 | 16 | 84154730 | frameshift variant | -/G | delins | 2 | |||
| rs267607226 | 1.000 | 0.120 | 16 | 84159725 | stop gained | C/A | snv | 7.0E-06 | 1 |