Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750671 | 0.790 | 0.240 | 21 | 25891858 | missense variant | G/C | snv | 8 | |||
rs63751039 | 0.776 | 0.200 | 21 | 25891855 | missense variant | T/C | snv | 8 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750671 | 0.790 | 0.240 | 21 | 25891858 | missense variant | G/C | snv | 8 | |||
rs63751039 | 0.776 | 0.200 | 21 | 25891855 | missense variant | T/C | snv | 8 |