Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12489828 | 3 | 52532998 | intron variant | G/T | snv | 0.51 | 4 | ||||
rs56116382 | 3 | 49568755 | intron variant | A/C | snv | 0.19 | 2 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12489828 | 3 | 52532998 | intron variant | G/T | snv | 0.51 | 4 | ||||
rs56116382 | 3 | 49568755 | intron variant | A/C | snv | 0.19 | 2 |