Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1569301036 | 0.827 | 0.240 | X | 71397354 | missense variant | C/T | snv | 17 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1569301036 | 0.827 | 0.240 | X | 71397354 | missense variant | C/T | snv | 17 |