Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs773641005 | 0.742 | 0.240 | 16 | 58723829 | missense variant | T/C | snv | 14 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs773641005 | 0.742 | 0.240 | 16 | 58723829 | missense variant | T/C | snv | 14 |