Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9467626 | 0.882 | 0.160 | 6 | 25873518 | intron variant | C/A | snv | 7.3E-02 | 4 | ||
rs13199775 | 0.882 | 0.160 | 6 | 25828554 | intron variant | A/T | snv | 7.4E-02 | 3 | ||
rs6939997 | 0.882 | 0.160 | 6 | 25820996 | intron variant | C/T | snv | 7.0E-02 | 3 | ||
rs9461219 | 0.882 | 0.160 | 6 | 25836699 | intron variant | C/G;T | snv | 3 |