Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10757272 | 0.851 | 0.160 | 9 | 22088261 | intron variant | C/T | snv | 0.41 | 3 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10757272 | 0.851 | 0.160 | 9 | 22088261 | intron variant | C/T | snv | 0.41 | 3 |