Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs886043613 | 0.925 | 0.080 | 4 | 1801519 | missense variant | C/T | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs886043613 | 0.925 | 0.080 | 4 | 1801519 | missense variant | C/T | snv | 4 |