| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
| rs12138950 | 0.925 | 0.040 | 1 | 19512621 | intron variant | A/C | snv | 5.4E-03 | 3 | ||
| rs2983514 | 0.925 | 0.040 | 6 | 165636631 | intron variant | A/G | snv | 0.34 | 2 |