Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12198986 | 6 | 7719826 | regulatory region variant | G/A | snv | 0.37 | 3 | ||||
rs7916441 | 10 | 79165820 | intron variant | G/C | snv | 0.39 | 2 | ||||
rs8067165 | 17 | 8128618 | upstream gene variant | C/A;G;T | snv | 3 | |||||
rs7155279 | 14 | 92019537 | intron variant | G/A;T | snv | 3 |