Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387907281 | 0.752 | 0.280 | 19 | 41970284 | missense variant | C/T | snv | 13 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387907281 | 0.752 | 0.280 | 19 | 41970284 | missense variant | C/T | snv | 13 |