Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10906522 | 1.000 | 0.080 | 10 | 13865236 | intron variant | T/A;C | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10906522 | 1.000 | 0.080 | 10 | 13865236 | intron variant | T/A;C | snv | 1 |