| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4738296 | 1.000 | 0.040 | 8 | 72945304 | upstream gene variant | A/C | snv | 7.9E-02 | 1 | ||
| rs7228576 | 1.000 | 0.040 | 18 | 10408495 | intron variant | C/T | snv | 0.19 | 1 | ||
| rs9864529 | 1.000 | 0.040 | 3 | 188387268 | intron variant | G/A | snv | 0.52 | 1 | ||
| rs7099812 | 1.000 | 0.040 | 10 | 19689469 | intron variant | T/G | snv | 0.41 | 1 | ||
| rs1431704 | 1.000 | 0.040 | 18 | 39273770 | intron variant | T/C | snv | 7.0E-02 | 1 | ||
| rs12348691 | 0.925 | 0.120 | 9 | 97846400 | intron variant | G/A | snv | 0.63 | 1 | ||
| rs17479692 | 1.000 | 0.040 | 10 | 89528702 | intron variant | T/G | snv | 9.3E-02 | 1 | ||
| rs10760706 | 1.000 | 0.040 | 9 | 99961410 | intron variant | C/T | snv | 0.69 | 1 |