| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1127354 | 0.667 | 0.400 | 20 | 3213196 | missense variant | C/A;G | snv | 7.5E-02 | 26 | ||
| rs1227149616 | 1.000 | 0.080 | 20 | 3218525 | stop gained | C/T | snv | 4.0E-06 | 1 | ||
| rs1381781375 | 1.000 | 0.080 | 20 | 3215286 | frameshift variant | G/- | delins | 1 | |||
| rs1568509937 | 1.000 | 0.080 | 20 | 3213171 | frameshift variant | -/G | delins | 1 |