Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1555575860 | 0.732 | 0.240 | 16 | 70496367 | missense variant | C/G;T | snv | 31 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1555575860 | 0.732 | 0.240 | 16 | 70496367 | missense variant | C/G;T | snv | 31 |