Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1085308045 | 0.807 | 0.160 | 10 | 87933128 | missense variant | C/G;T | snv | 8 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1085308045 | 0.807 | 0.160 | 10 | 87933128 | missense variant | C/G;T | snv | 8 |