Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113125564 | 19 | 47092874 | intron variant | T/C | snv | 2.9E-02 | 1 | ||||
rs17716478 | 19 | 47097336 | intron variant | C/T | snv | 5.3E-02 | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113125564 | 19 | 47092874 | intron variant | T/C | snv | 2.9E-02 | 1 | ||||
rs17716478 | 19 | 47097336 | intron variant | C/T | snv | 5.3E-02 | 1 |