Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10489276 | 1.000 | 0.040 | 1 | 172893799 | intron variant | C/T | snv | 0.31 | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10489276 | 1.000 | 0.040 | 1 | 172893799 | intron variant | C/T | snv | 0.31 | 1 |