Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6977416 | 7 | 150845623 | intron variant | G/A | snv | 0.48 | 2 | ||||
rs73148102 | 7 | 65973877 | intron variant | G/A | snv | 0.14 | 2 | ||||
rs7916441 | 10 | 79165820 | intron variant | G/C | snv | 0.39 | 2 | ||||
rs7926971 | 11 | 12676493 | intron variant | A/G | snv | 0.41 | 2 |