| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs74315320 | 0.925 | 0.120 | 1 | 34785183 | missense variant | A/G | snv | 2 | |||
| rs879255246 | 0.925 | 0.120 | 2 | 26484568 | missense variant | C/G;T | snv | 4.0E-06 | 2 | ||
| rs772264564 | 1.000 | 0.120 | 13 | 20189117 | stop gained | A/T | snv | 4.0E-06 | 1 | ||
| rs770247378 | 1.000 | 0.120 | 1 | 34785183 | inframe deletion | ATT/- | del | 1 |