Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7916441 | 10 | 79165820 | intron variant | G/C | snv | 0.39 | 2 | ||||
rs7926971 | 11 | 12676493 | intron variant | A/G | snv | 0.41 | 2 | ||||
rs8067165 | 17 | 8128618 | upstream gene variant | C/A;G;T | snv | 3 | |||||
rs9435733 | 1 | 16981759 | intron variant | T/C | snv | 0.41 | 3 |