| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1555727493 | 0.742 | 0.480 | 19 | 35718020 | frameshift variant | -/GGCGGGCGGCGGC | delins | 46 | |||
| rs1555731819 | 0.807 | 0.200 | 19 | 35729980 | missense variant | G/T | snv | 26 | |||
| rs1555734923 | 19 | 35738078 | stop gained | C/T | snv | 1 | |||||
| rs1555732987 | 19 | 35732782 | frameshift variant | -/GCACGCCTCCTTCGGGGCCAGG | delins | 1 | |||||
| rs1555729045 | 19 | 35721772 | stop gained | C/T | snv | 1 | |||||
| rs1057519283 | 1.000 | 19 | 35721037 | stop gained | C/T | snv | 1 | ||||
| rs1057519282 | 1.000 | 19 | 35719502 | frameshift variant | -/C | delins | 1 | ||||
| rs1057519284 | 1.000 | 19 | 35728145 | stop gained | C/A;T | snv | 1 | ||||
| rs1057519281 | 1.000 | 19 | 35721775 | stop gained | C/T | snv | 1 | ||||
| rs1057519279 | 1.000 | 19 | 35720980 | stop gained | C/T | snv | 1 | ||||
| rs1057519280 | 1.000 | 19 | 35733761 | splice acceptor variant | A/G | snv | 1 | ||||
| rs779863547 | 1.000 | 19 | 35730766 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | ||
| rs1568377293 | 1.000 | 19 | 35728824 | missense variant | C/T | snv | 1 | ||||
| rs763183959 | 1.000 | 19 | 35719862 | frameshift variant | C/-;CC | delins | 1 | ||||
| rs1057519278 | 1.000 | 19 | 35732955 | frameshift variant | C/- | del | 1 | ||||
| rs1568379151 | 1.000 | 19 | 35730765 | stop gained | C/T | snv | 1 |