Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs111906841 | 3 | 141242812 | intron variant | A/G | snv | 1.5E-02 | 1 | ||||
rs1346408 | 3 | 141353447 | intron variant | C/T | snv | 0.55 | 1 | ||||
rs1567558 | 3 | 141289281 | intron variant | A/G | snv | 0.50 | 2 | ||||
rs28721484 | 3 | 141334437 | intron variant | C/T | snv | 0.22 | 2 | ||||
rs34655123 | 3 | 141348246 | intron variant | A/G | snv | 4.7E-02 | 1 | ||||
rs55768579 | 3 | 141340945 | intron variant | GA/- | delins | 1.3E-03 | 1 | ||||
rs9866391 | 1.000 | 0.040 | 3 | 141357242 | intron variant | T/C | snv | 0.41 | 1 |