Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28900396 | 2 | 233761914 | intron variant | T/C | snv | 6.4E-02 | 3 | ||||
rs28900402 | 2 | 233767766 | intron variant | C/T | snv | 2.7E-02 | 1 |