| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587777585 | 0.882 | 6 | 30918851 | missense variant | C/G;T | snv | 2.4E-05 | 6 | |||
| rs139515727 | 1.000 | 6 | 30915985 | missense variant | C/T | snv | 3.2E-05 | 1.0E-04 | 2 | ||
| rs1554268077 | 1.000 | 6 | 30920731 | inframe deletion | GGG/- | delins | 1 | ||||
| rs587777583 | 1.000 | 6 | 30918886 | missense variant | G/A | snv | 1 | ||||
| rs587777584 | 1.000 | 6 | 30921976 | missense variant | C/A | snv | 4.1E-06 | 1 | |||
| rs775439829 | 1.000 | 6 | 30920670 | missense variant | G/A;C | snv | 7.0E-06 | 1 |