Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2066808 | 0.807 | 0.280 | 12 | 56344189 | intron variant | A/G | snv | 0.21 | 2 | ||
rs2066807 | 0.925 | 0.080 | 12 | 56346898 | missense variant | C/G | snv | 4.9E-02 | 4.6E-02 | 1 | |
rs2066819 | 0.925 | 0.040 | 12 | 56356420 | intron variant | C/T | snv | 4.9E-02 | 4.5E-02 | 1 |