Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs67687202 | 1.000 | 0.080 | 9 | 99147870 | intron variant | TCTTT/- | delins | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs67687202 | 1.000 | 0.080 | 9 | 99147870 | intron variant | TCTTT/- | delins | 1 |