| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913660 | 1.000 | 11 | 67611511 | missense variant | C/T | snv | 3.2E-05 | 6.3E-05 | 1 | ||
| rs121913659 | 0.925 | 0.040 | 11 | 67612225 | missense variant | C/T | snv | 1.2E-05 | 3.5E-05 | 1 | |
| rs121913661 | 1.000 | 11 | 67610510 | missense variant | G/A | snv | 1.4E-05 | 1 |