Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913105 | 0.653 | 0.600 | 4 | 1806163 | missense variant | A/C;T | snv | 4 | |||
rs121913479 | 0.763 | 0.280 | 4 | 1804362 | missense variant | G/A;T | snv | 4.0E-06 | 4 | ||
rs121913482 | 0.630 | 0.680 | 4 | 1801837 | missense variant | C/T | snv | 4 | |||
rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 4 | ||
rs78311289 | 0.689 | 0.440 | 4 | 1806162 | missense variant | A/C;G | snv | 4.0E-06 | 4 | ||
rs121913484 | 0.851 | 0.240 | 4 | 1804365 | missense variant | A/T | snv | 2 | |||
rs121913485 | 0.716 | 0.400 | 4 | 1804372 | missense variant | A/G | snv | 2 | |||
rs28931614 | 0.672 | 0.520 | 4 | 1804392 | missense variant | G/A;C | snv | 2 | |||
rs869320694 | 0.742 | 0.520 | 8 | 38414790 | missense variant | T/C | snv | 1 | |||
rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 1 |