Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587783772 | 0.776 | 0.200 | X | 150659665 | missense variant | G/A;T | snv | 14 | |||
rs1057516031 | 1.000 | 0.080 | X | 150598681 | stop gained | G/T | snv | 3 | |||
rs132630304 | 0.882 | 0.080 | X | 150598660 | missense variant | C/G;T | snv | 3 | |||
rs587783752 | 0.925 | 0.080 | X | 150657854 | frameshift variant | AA/-;AAA | delins | 2 | |||
rs132630302 | 1.000 | 0.080 | X | 150641306 | missense variant | A/G | snv | 1 | |||
rs132630303 | 1.000 | 0.080 | X | 150657957 | missense variant | A/G | snv | 1 | |||
rs132630305 | 1.000 | 0.080 | X | 150645725 | missense variant | C/T | snv | 1 | |||
rs132630306 | 1.000 | 0.080 | X | 150641410 | stop gained | C/T | snv | 1 | |||
rs132630307 | 1.000 | 0.080 | X | 150638967 | missense variant | G/A | snv | 1 | |||
rs1557413092 | 1.000 | 0.080 | X | 150614700 | splice donor variant | G/A | snv | 1 | |||
rs1557413783 | 1.000 | 0.080 | X | 150638963 | frameshift variant | T/- | del | 1 | |||
rs1557414513 | 1.000 | 0.080 | X | 150657943 | frameshift variant | -/T | delins | 1 | |||
rs1569565497 | 1.000 | 0.080 | X | 150641333 | missense variant | A/C | snv | 1 | |||
rs1569565525 | 1.000 | 0.080 | X | 150657971 | missense variant | G/A | snv | 1 | |||
rs34119065 | 1.000 | 0.080 | X | 150671572 | frameshift variant | C/-;CC | delins | 1 | |||
rs397518445 | 1.000 | 0.080 | X | 150659654 | intron variant | A/G | snv | 1 | |||
rs398123274 | 1.000 | 0.080 | X | 150645692 | missense variant | T/C | snv | 1 | |||
rs398123275 | 1.000 | 0.080 | X | 150596504 | stop gained | C/T | snv | 1 | |||
rs587783750 | 1.000 | 0.080 | X | 150649884 | missense variant | T/C | snv | 1 | |||
rs587783751 | 1.000 | 0.080 | X | 150649902 | splice donor variant | G/A;C | snv | 1 | |||
rs587783753 | 1.000 | 0.080 | X | 150596543 | stop gained | C/T | snv | 9.5E-06 | 1 | ||
rs587783754 | 1.000 | 0.080 | X | 150657887 | missense variant | C/G | snv | 1 | |||
rs587783755 | 1.000 | 0.080 | X | 150657899 | missense variant | G/A | snv | 1 | |||
rs587783756 | 1.000 | 0.080 | X | 150657903 | stop gained | G/A | snv | 1 | |||
rs587783757 | 1.000 | 0.080 | X | 150657904 | stop gained | G/A | snv | 1 |