Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137853924 | 0.851 | 0.200 | 2 | 208128343 | missense variant | C/A;T | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137853924 | 0.851 | 0.200 | 2 | 208128343 | missense variant | C/A;T | snv | 4 |