| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387906846 | 0.807 | 0.280 | 1 | 26773716 | stop gained | C/G;T | snv | 19 | |||
| rs1557570794 | 0.742 | 0.120 | 1 | 26697152 | frameshift variant | -/GCCGCCTCCCTCCTCCAGCGCC | delins | 15 | |||
| rs1557612048 | 0.807 | 0.200 | 1 | 26767868 | missense variant | T/C | snv | 11 | |||
| rs1485978447 | 1.000 | 1 | 26779062 | stop gained | C/A;T | snv | 1 | ||||
| rs1553146165 | 1.000 | 1 | 26697317 | frameshift variant | CTACCAGGGCTACCCCGGGG/- | delins | 1 | ||||
| rs1553153291 | 1.000 | 1 | 26775086 | frameshift variant | -/A | delins | 1 | ||||
| rs1557591264 | 1.000 | 1 | 26729861 | stop gained | C/T | snv | 1 | ||||
| rs1557620758 | 1.000 | 1 | 26780032 | frameshift variant | AAGTG/- | del | 1 | ||||
| rs387906845 | 1.000 | 1 | 26766246 | stop gained | C/T | snv | 1 | ||||
| rs797045262 | 1.000 | 1 | 26696422 | frameshift variant | AGCAGCCTGGGCAACCCGCCGCCGCC/- | delins | 1 | ||||
| rs797045263 | 1.000 | 1 | 26696794 | frameshift variant | G/- | delins | 1 | ||||
| rs797045264 | 1.000 | 1 | 26779036 | missense variant | T/C | snv | 1 |