Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7775055 | 0.790 | 0.200 | 6 | 32690139 | TF binding site variant | T/C | snv | 6.2E-02 | 7 | ||
rs7909519 | 0.807 | 0.120 | 10 | 6047878 | intron variant | T/G | snv | 7.2E-02 | 6 | ||
rs79893749 | 0.807 | 0.120 | 3 | 46212159 | intron variant | C/T | snv | 0.10 | 6 | ||
rs8129030 | 0.807 | 0.120 | 21 | 35340290 | intron variant | T/A;G | snv | 0.72 | 7 | ||
rs9532434 | 0.807 | 0.120 | 13 | 39781776 | intron variant | T/A;C | snv | 8 | |||
rs34536443 | 0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 | 25 |