Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1556022962 | X | 133304782 | missense variant | C/T | snv | 1 | |||||
rs1048369 | 0.882 | 0.160 | X | 133303309 | missense variant | G/A | snv | 0.33 | 0.38 | 4 | |
rs1556022641 | 1.000 | 0.200 | X | 133303022 | stop gained | G/A | snv | 1 | |||
rs1556022644 | 1.000 | 0.200 | X | 133303052 | stop gained | C/A | snv | 1 | |||
rs1556025980 | 1.000 | 0.200 | X | 133324154 | frameshift variant | -/T | delins | 1 | |||
rs1556028269 | 1.000 | 0.200 | X | 133339186 | frameshift variant | C/- | del | 1 | |||
rs1569339879 | 1.000 | 0.200 | X | 133303016 | frameshift variant | -/GCAC | delins | 1 | |||
rs1569341521 | 1.000 | 0.200 | X | 133311393 | frameshift variant | G/- | delins | 1 |