Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10852606 | 0.882 | 0.040 | 16 | 50094961 | intron variant | T/A;C | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10852606 | 0.882 | 0.040 | 16 | 50094961 | intron variant | T/A;C | snv | 4 |