| 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 | ||
| rs597808 | 0.742 | 0.200 | 12 | 111535554 | intron variant | A/G | snv | 0.67 | 19 | ||
| rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 10 | |||
| rs2925979 | 1.000 | 0.080 | 16 | 81501185 | intron variant | T/A;C | snv | 10 | |||
| rs17451107 | 3 | 157079820 | upstream gene variant | T/C | snv | 0.38 | 7 | ||||
| rs2071449 | 12 | 54034227 | intron variant | C/A;T | snv | 0.35; 4.2E-06 | 4 |