Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17757541 | 0.827 | 0.240 | 18 | 63212453 | intron variant | C/G;T | snv | 7 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17757541 | 0.827 | 0.240 | 18 | 63212453 | intron variant | C/G;T | snv | 7 |