Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs4291 | 0.724 | 0.400 | 17 | 63476833 | upstream gene variant | T/A;C | snv | 20 | |||
rs530390117 | 0.882 | 0.240 | 1 | 172659460 | missense variant | T/C | snv | 3.0E-04 | 2.1E-05 | 3 | |
rs3771863 | 0.925 | 0.240 | 2 | 75192588 | intron variant | C/T | snv | 0.30 | 2 |