Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs797045203 | 1.000 | 0.040 | 20 | 58909540 | missense variant | C/A | snv | 1 | |||
rs863224876 | 0.925 | 0.120 | 20 | 58909991 | stop gained | C/T | snv | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs797045203 | 1.000 | 0.040 | 20 | 58909540 | missense variant | C/A | snv | 1 | |||
rs863224876 | 0.925 | 0.120 | 20 | 58909991 | stop gained | C/T | snv | 2 |