Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs866294686 | 0.683 | 0.480 | 10 | 102657073 | stop gained | C/A;T | snv | 43 | |||
rs1555462347 | 0.716 | 0.520 | 16 | 8901028 | frameshift variant | CT/- | delins | 34 | |||
rs1057524820 | 0.776 | 0.280 | 12 | 51765746 | missense variant | G/A;T | snv | 33 | |||
rs752746786 | 0.742 | 0.560 | 1 | 1806503 | missense variant | A/C;G;T | snv | 4.0E-06 | 30 | ||
rs771379232 | 0.790 | 0.120 | 15 | 79845338 | stop gained | G/A | snv | 2.0E-05 | 3.5E-05 | 15 | |
rs753635972 | 0.790 | 0.120 | 15 | 79845388 | missense variant | C/T | snv | 3.2E-05 | 2.1E-05 | 15 | |
rs869312825 | 0.827 | 0.120 | 1 | 1804548 | start lost | T/C | snv | 11 | |||
rs869312822 | 0.827 | 0.200 | 1 | 1806514 | missense variant | A/C | snv | 8 | |||
rs587779411 | 0.851 | 0.160 | 8 | 1780498 | missense variant | C/G;T | snv | 4.0E-06 | 5 | ||
rs143730802 | 0.882 | 0.160 | 8 | 1771055 | start lost | A/G | snv | 1.2E-05 | 7.0E-06 | 4 |