Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs672601368 | 0.827 | 0.160 | 2 | 240785062 | missense variant | C/G;T | snv | 10 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs672601368 | 0.827 | 0.160 | 2 | 240785062 | missense variant | C/G;T | snv | 10 |