Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs138740 | 0.882 | 0.160 | 22 | 35303589 | intron variant | C/T | snv | 0.51 | 3 | ||
rs138747 | 1.000 | 0.160 | 22 | 35304495 | intron variant | A/C;T | snv | 1 | |||
rs138777 | 22 | 35315105 | intron variant | A/G | snv | 0.51 | 1 | ||||
rs138788 | 1.000 | 0.040 | 22 | 35333728 | intron variant | G/A | snv | 0.49 | 1 |