Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1131692231 | 0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv | 13 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1131692231 | 0.827 | 0.280 | 5 | 157294834 | missense variant | C/T | snv | 13 |