Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913468 | 0.827 | 0.160 | 17 | 39724008 | missense variant | G/A;C;T | snv | 5 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913468 | 0.827 | 0.160 | 17 | 39724008 | missense variant | G/A;C;T | snv | 5 |