Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs661171 | 11 | 110145794 | intron variant | T/G | snv | 0.69 | 5 | ||||
rs10789752 | 11 | 110109220 | intron variant | T/A;C | snv | 1 | |||||
rs689183 | 11 | 110141418 | intron variant | G/T | snv | 0.74 | 1 | ||||
rs746463 | 11 | 110125219 | intron variant | C/T | snv | 0.71 | 1 |