Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs730881756 | 0.925 | 0.080 | 2 | 47445653 | missense variant | A/C;G | snv | 4.0E-06 | 2 | ||
rs869312768 | 0.925 | 0.160 | 2 | 47429865 | frameshift variant | -/TT | delins | 2 | |||
rs1553368590 | 0.882 | 0.200 | 2 | 47475097 | missense variant | T/A | snv | 3 | |||
rs587779157 | 0.827 | 0.240 | 2 | 47408486 | inframe deletion | GAAGTT/- | delins | 6 | |||
rs63751207 | 0.851 | 0.240 | 2 | 47466718 | missense variant | G/A;C;T | snv | 8.0E-06 | 6 | ||
rs1114167806 | 0.827 | 0.200 | 2 | 47463096 | stop gained | ATGA/-;ATGAATGA | delins | 7 | |||
rs4987188 | 0.790 | 0.200 | 2 | 47416318 | missense variant | G/A;T | snv | 1.3E-02; 2.0E-05 | 11 | ||
rs63750875 | 0.742 | 0.280 | 2 | 47475171 | missense variant | G/A;C | snv | 1.6E-05 | 15 |