Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10009128 | 0.925 | 0.040 | 4 | 19511508 | intron variant | C/T | snv | 0.34 | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10009128 | 0.925 | 0.040 | 4 | 19511508 | intron variant | C/T | snv | 0.34 | 2 |