Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13112725 | 4 | 105990585 | intron variant | G/C | snv | 0.70 | 2 | ||||
rs56388530 | 4 | 105989801 | intron variant | C/A;T | snv | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13112725 | 4 | 105990585 | intron variant | G/C | snv | 0.70 | 2 | ||||
rs56388530 | 4 | 105989801 | intron variant | C/A;T | snv | 2 |