Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912655 | 0.724 | 0.400 | 17 | 7674238 | missense variant | C/A;G;T | snv | 15 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912655 | 0.724 | 0.400 | 17 | 7674238 | missense variant | C/A;G;T | snv | 15 |