Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121907900 | 0.763 | 0.200 | 11 | 32392020 | missense variant | G/A | snv | 11 | |||
rs121907906 | 0.776 | 0.320 | 11 | 32392717 | stop gained | G/A | snv | 8 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121907900 | 0.763 | 0.200 | 11 | 32392020 | missense variant | G/A | snv | 11 | |||
rs121907906 | 0.776 | 0.320 | 11 | 32392717 | stop gained | G/A | snv | 8 |