Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6058227 | 20 | 35308144 | intron variant | C/T | snv | 0.15 | 2 | ||||
rs6060369 | 20 | 35319358 | intron variant | T/C | snv | 0.49 | 1 | ||||
rs6060373 | 0.925 | 0.200 | 20 | 35326405 | intron variant | A/G | snv | 0.49 | 1 | ||
rs6088792 | 20 | 35321981 | intron variant | C/T | snv | 0.26 | 1 | ||||
rs6088813 | 20 | 35387378 | intron variant | C/A | snv | 0.54 | 1 |