Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs67806247 | 19 | 1014539 | intron variant | TGATGGGGCG/-;TGATGGGGCGTGATGGGGCG | delins | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs67806247 | 19 | 1014539 | intron variant | TGATGGGGCG/-;TGATGGGGCGTGATGGGGCG | delins | 2 |