| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 22 | |||
| rs13412535 | 2 | 224010157 | intron variant | G/A | snv | 0.17 | 5 | ||||
| rs4841899 | 9 | 134532566 | intron variant | T/C | snv | 0.32 | 2 | ||||
| rs184905639 | 8 | 33229938 | upstream gene variant | G/A | snv | 3.8E-03 | 1 | ||||
| rs80271436 | 9 | 133022383 | downstream gene variant | G/A | snv | 4.7E-02 | 1 | ||||
| rs1557570 | 1 | 169538606 | intron variant | G/T | snv | 0.30 | 1 | ||||
| rs1568119 | 8 | 33385679 | intron variant | C/T | snv | 4.5E-02 | 1 | ||||
| rs200393053 | 8 | 32736709 | intron variant | T/-;TT | delins | 1 |