| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
| rs2477686 | 0.807 | 0.040 | 1 | 2461209 | intron variant | G/C | snv | 0.64 | 7 | ||
| rs199696526 | 0.882 | 0.040 | 16 | 4786006 | missense variant | G/A | snv | 1.2E-04 | 5.6E-05 | 3 | |
| rs215702 | 0.925 | 0.040 | 7 | 32360046 | intron variant | G/A | snv | 0.57 | 3 | ||
| rs371195126 | 0.882 | 0.040 | 16 | 4783690 | missense variant | C/G;T | snv | 2.4E-05 | 3 |