| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1556779417 | 1.000 | X | 47181541 | frameshift variant | GT/- | delins | 3 | ||||
| rs1131690789 | 1.000 | X | 47181316 | frameshift variant | AG/- | delins | 2 | ||||
| rs1556770954 | 1.000 | 0.160 | X | 47169456 | frameshift variant | C/- | del | 1 | |||
| rs1556778986 | 1.000 | 0.160 | X | 47181214 | splice acceptor variant | G/A | snv | 1 | |||
| rs267607000 | 1.000 | 0.160 | X | 47180493 | stop gained | G/A | snv | 1 | |||
| rs868917893 | X | 47171183 | missense variant | G/T | snv | 6.0E-06 | 1 | ||||
| rs886044715 | 1.000 | 0.160 | X | 47182268 | frameshift variant | -/A | delins | 1 | |||
| rs886044718 | 1.000 | 0.160 | X | 47173143 | stop gained | C/T | snv | 1 |