Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908212 | 0.732 | 0.160 | 19 | 13303877 | missense variant | G/A | snv | 14 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908212 | 0.732 | 0.160 | 19 | 13303877 | missense variant | G/A | snv | 14 |