Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2228391 | 0.882 | 0.160 | 6 | 32829996 | missense variant | T/C | snv | 1.3E-02 | 3.9E-03 | 3 | |
rs114291795 | 0.925 | 0.040 | 6 | 31409863 | intron variant | C/G | snv | 3.0E-02 | 2 | ||
rs185386680 | 0.925 | 0.040 | 6 | 31207153 | downstream gene variant | A/G | snv | 1.2E-03 | 2 |