| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1421405659 | 0.851 | 0.360 | 12 | 101642529 | missense variant | T/C;G | snv | 13 | |||
| rs564856283 | 12 | 101642495 | missense variant | G/A;C | snv | 3.2E-05 | 3 | ||||
| rs1555242493 | 1.000 | 0.080 | 12 | 101653159 | missense variant | G/C | snv | 1 | |||
| rs387906657 | 0.925 | 0.080 | 12 | 101642459 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs397515422 | 1.000 | 12 | 101644783 | stop gained | C/T | snv | 4.0E-06 | 7.0E-06 | 1 |