Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1568523935 | 0.776 | 0.240 | 19 | 19105656 | stop gained | C/G | snv | 20 | |||
rs397514698 | 0.667 | 0.400 | 9 | 77797577 | missense variant | C/T | snv | 41 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1568523935 | 0.776 | 0.240 | 19 | 19105656 | stop gained | C/G | snv | 20 | |||
rs397514698 | 0.667 | 0.400 | 9 | 77797577 | missense variant | C/T | snv | 41 |