Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387906760 | 0.790 | 0.200 | 2 | 190995184 | missense variant | C/T | snv | 13 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387906760 | 0.790 | 0.200 | 2 | 190995184 | missense variant | C/T | snv | 13 |