Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs143326447 | 0.925 | 0.080 | 2 | 111511155 | intron variant | T/C | snv | 0.11 | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs143326447 | 0.925 | 0.080 | 2 | 111511155 | intron variant | T/C | snv | 0.11 | 4 |