Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397516827 | 0.882 | 0.160 | 3 | 12604194 | missense variant | G/A;C;T | snv | 9 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397516827 | 0.882 | 0.160 | 3 | 12604194 | missense variant | G/A;C;T | snv | 9 |