| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 73 | |||
| rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 73 | |||
| rs121917757 | 0.851 | 0.200 | 11 | 534259 | stop gained | G/A;T | snv | 1.2E-05 | 4 | ||
| rs121917756 | 0.925 | 0.120 | 11 | 533869 | missense variant | C/T | snv | 2 |