Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs869025340 | 0.925 | 0.160 | 7 | 140777032 | missense variant | A/C;G;T | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs869025340 | 0.925 | 0.160 | 7 | 140777032 | missense variant | A/C;G;T | snv | 4 |