Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17153249 | 1.000 | 0.040 | 10 | 125599721 | intron variant | C/T | snv | 8.3E-02 | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17153249 | 1.000 | 0.040 | 10 | 125599721 | intron variant | C/T | snv | 8.3E-02 | 1 |