Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs35993099 | 10 | 45511519 | intron variant | T/A | snv | 6.2E-02 | 2 | ||||
| rs34285816 | 10 | 45481403 | intron variant | G/A | snv | 6.3E-02 | 1 | ||||
| rs112297763 | 10 | 45573988 | intron variant | T/C | snv | 6.5E-02 | 1 | ||||
| rs963029 | 10 | 45467939 | intron variant | C/T | snv | 0.24 | 1 |