Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61755771 | 0.827 | 0.160 | 6 | 42722199 | stop gained | G/A | snv | 1.6E-05 | 1.4E-05 | 5 | |
rs61755792 | 0.763 | 0.160 | 6 | 42721821 | missense variant | G/A;C | snv | 10 | |||
rs121918563 | 0.827 | 0.120 | 6 | 42721781 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 | 6 | |
rs121918567 | 0.807 | 0.080 | 6 | 42704609 | missense variant | C/A;T | snv | 4.0E-06 | 6 | ||
rs61755798 | 0.827 | 0.080 | 6 | 42704564 | missense variant | G/A;C | snv | 6 | |||
rs61755787 | 0.882 | 0.120 | 6 | 42721866 | missense variant | C/T | snv | 5 | |||
rs61755781 | 0.851 | 0.080 | 6 | 42721913 | missense variant | T/C | snv | 4 | |||
rs527236098 | 0.925 | 0.080 | 6 | 42721836 | missense variant | C/T | snv | 2 | |||
rs61755789 | 0.925 | 0.080 | 6 | 42721835 | missense variant | C/T | snv | 2 | |||
rs61755802 | 1.000 | 0.040 | 6 | 42704556 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs61755809 | 0.925 | 0.080 | 6 | 42704535 | missense variant | G/A;T | snv | 4.0E-06 | 2 | ||
rs61755774 | 1.000 | 0.040 | 6 | 42722133 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs61755810 | 1.000 | 0.040 | 6 | 42704534 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs61748429 | 1.000 | 0.040 | 6 | 42698438 | frameshift variant | CA/- | del | 1 | |||
rs672601326 | 1.000 | 0.040 | 6 | 42721913 | frameshift variant | -/AGTA | delins | 1 | |||
rs61755786 | 0.925 | 0.080 | 6 | 42721872 | inframe deletion | TTC/- | delins | 2 |