Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913512 | 0.851 | 0.120 | 4 | 54728055 | missense variant | A/C;G | snv | 6 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913512 | 0.851 | 0.120 | 4 | 54728055 | missense variant | A/C;G | snv | 6 |