Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs732609 | 0.827 | 0.160 | 2 | 1496155 | missense variant | A/C;G | snv | 0.43 | 5 | ||
rs2069566 | 0.851 | 0.160 | 8 | 133017940 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 4 | |
rs57659670 | 0.925 | 0.120 | 15 | 45106240 | missense variant | T/C | snv | 9.8E-02 | 0.17 | 2 | |
rs746165975 | 0.925 | 0.120 | 15 | 45106254 | frameshift variant | -/T | delins | 4.0E-06 | 2 | ||
rs758368355 | 1.000 | 0.120 | 2 | 1477452 | missense variant | C/A;T | snv | 8.3E-06 | 1 |