| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
| rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
| rs8067165 | 17 | 8128618 | upstream gene variant | C/A;G;T | snv | 3 | |||||
| rs2199036 | 16 | 30995651 | intron variant | C/T | snv | 0.37 | 2 | ||||
| rs933738 | 12 | 49549339 | intron variant | A/C;G | snv | 2 |