Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113994109 | 0.827 | 0.200 | 13 | 110179370 | missense variant | C/T | snv | 5 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113994109 | 0.827 | 0.200 | 13 | 110179370 | missense variant | C/T | snv | 5 |