| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1255388379 | 20 | 64092838 | missense variant | G/A | snv | 2.1E-05 | 1 | ||||
| rs1262930152 | 1 | 31577384 | missense variant | G/A;T | snv | 8.0E-06 | 1 | ||||
| rs3735451 | 7 | 99758352 | intron variant | T/C | snv | 0.31 | 1 | ||||
| rs3743484 | 15 | 74752059 | intron variant | G/C | snv | 3.7E-02 | 1 | ||||
| rs4646778 | 12 | 111797979 | intron variant | C/A | snv | 0.18 | 1 | ||||
| rs750891770 | 1 | 31583538 | missense variant | G/A | snv | 2.8E-05 | 2.1E-05 | 1 |