| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs878853164 | 1.000 | 0.160 | 11 | 68157849 | stop gained | C/A | snv | 4.0E-06 | 5 | ||
| rs1555028206 | 1.000 | 11 | 68171705 | stop gained | G/A | snv | 2 | ||||
| rs1555027828 | 1.000 | 11 | 68171022 | missense variant | A/C | snv | 1 | ||||
| rs114727354 | 1.000 | 11 | 68173898 | stop gained | G/A;T | snv | 4.4E-03 | 1.4E-02 | 1 | ||
| rs1555023232 | 1.000 | 11 | 68158788 | frameshift variant | CT/- | delins | 1 | ||||
| rs1555028154 | 1.000 | 11 | 68171638 | frameshift variant | A/- | del | 1 | ||||
| rs1555034768 | 1.000 | 11 | 68185834 | frameshift variant | G/- | delins | 1 | ||||
| rs1565240833 | 1.000 | 11 | 68185870 | frameshift variant | G/- | delins | 1 |