| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121434618 | 0.827 | 0.200 | X | 40075092 | missense variant | G/A;C | snv | 5.6E-06 | 7 | ||
| rs121434619 | 1.000 | 0.120 | X | 40072420 | stop gained | G/A | snv | 1 | |||
| rs1555915744 | 1.000 | 0.120 | X | 40064393 | inframe deletion | GTCTCAGTG/- | delins | 1 | |||
| rs1555915763 | 1.000 | 0.120 | X | 40064427 | frameshift variant | TT/- | delins | 1 | |||
| rs1555915785 | 1.000 | 0.120 | X | 40064449 | frameshift variant | -/G | delins | 1 | |||
| rs1555915854 | 1.000 | 0.120 | X | 40064570 | frameshift variant | C/- | del | 1 | |||
| rs1555918014 | 1.000 | 0.120 | X | 40072857 | frameshift variant | CT/- | delins | 1 | |||
| rs1569146193 | 1.000 | 0.120 | X | 40062394 | splice acceptor variant | C/A | snv | 1 | |||
| rs730880013 | 1.000 | 0.120 | X | 40072733 | frameshift variant | G/- | del | 1 | |||
| rs730880034 | 1.000 | 0.120 | X | 40062259 | frameshift variant | TGGCA/- | delins | 1 | |||
| rs754807742 | 1.000 | 0.120 | X | 40075081 | missense variant | C/T | snv | 1.7E-05 | 9.6E-06 | 1 | |
| rs863224850 | 1.000 | 0.120 | X | 40062808 | stop gained | G/A | snv | 1 |