Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913506 | 0.677 | 0.320 | 4 | 54733154 | missense variant | G/A;C;T | snv | 24 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913506 | 0.677 | 0.320 | 4 | 54733154 | missense variant | G/A;C;T | snv | 24 |