Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs753635972 | 0.790 | 0.120 | 15 | 79845388 | missense variant | C/T | snv | 3.2E-05 | 2.1E-05 | 15 | |
rs771379232 | 0.790 | 0.120 | 15 | 79845338 | stop gained | G/A | snv | 2.0E-05 | 3.5E-05 | 15 | |
rs397507475 | 0.925 | 0.200 | 7 | 140778054 | missense variant | A/G | snv | 2 | |||
rs587777893 | 0.658 | 0.240 | 1 | 11128107 | missense variant | G/A;T | snv | 67 | |||
rs1554208945 | 0.752 | 0.240 | 6 | 87260207 | missense variant | A/C | snv | 26 | |||
rs1555968941 | 0.752 | 0.280 | 12 | 2653847 | missense variant | G/A;C | snv | 31 | |||
rs797046101 | 0.851 | 0.280 | X | 49076469 | stop gained | G/A | snv | 5 | |||
rs1555525115 | 0.851 | 0.360 | 16 | 89279567 | frameshift variant | GGCTTCGG/- | delins | 5 | |||
rs1557043622 | 0.695 | 0.400 | X | 48909843 | missense variant | C/A | snv | 46 |