Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs60600003 | 0.827 | 0.120 | 7 | 37342861 | intron variant | T/C;G | snv | 7 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs60600003 | 0.827 | 0.120 | 7 | 37342861 | intron variant | T/C;G | snv | 7 |