Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs377767347 | 0.742 | 0.520 | 18 | 51065549 | missense variant | G/A;C;T | snv | 14 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs377767347 | 0.742 | 0.520 | 18 | 51065549 | missense variant | G/A;C;T | snv | 14 |