Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057520006 | 0.752 | 0.240 | 17 | 7673799 | missense variant | A/C;G;T | snv | 12 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057520006 | 0.752 | 0.240 | 17 | 7673799 | missense variant | A/C;G;T | snv | 12 |