Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs36212733 | 1.000 | 0.040 | 10 | 122455695 | intron variant | T/C | snv | 0.23 | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs36212733 | 1.000 | 0.040 | 10 | 122455695 | intron variant | T/C | snv | 0.23 | 1 |