Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10863888 | 0.851 | 0.280 | 1 | 211329427 | intron variant | A/C;G;T | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10863888 | 0.851 | 0.280 | 1 | 211329427 | intron variant | A/C;G;T | snv | 4 |