Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912893 | 0.708 | 0.400 | 12 | 47983721 | stop gained | G/A;T | snv | 15 | |||
rs121912894 | 0.925 | 0.080 | 12 | 47993475 | missense variant | C/T | snv | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912893 | 0.708 | 0.400 | 12 | 47983721 | stop gained | G/A;T | snv | 15 | |||
rs121912894 | 0.925 | 0.080 | 12 | 47993475 | missense variant | C/T | snv | 2 |