Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908150 | 0.851 | 0.080 | 1 | 247424227 | stop gained | C/T | snv | 5 | |||
rs121908146 | 0.851 | 0.120 | 1 | 247424765 | missense variant | C/T | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908150 | 0.851 | 0.080 | 1 | 247424227 | stop gained | C/T | snv | 5 | |||
rs121908146 | 0.851 | 0.120 | 1 | 247424765 | missense variant | C/T | snv | 4 |