| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs867410737 | 0.708 | 0.440 | 19 | 1242559 | missense variant | C/T | snv | 6.7E-06 | 45 | ||
| rs1565679039 | 0.701 | 0.400 | 12 | 47983399 | stop gained | T/A | snv | 45 | |||
| rs1569309484 | 0.807 | 0.200 | X | 74591586 | missense variant | A/G | snv | 13 | |||
| rs1064795945 | 1.000 | 0.120 | 1 | 197102332 | frameshift variant | AAGT/- | delins | 5 | |||
| rs1064796738 | 1.000 | 0.240 | 10 | 92606655 | stop gained | C/T | snv | 5 |