| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2236648 | 0.925 | 0.080 | 11 | 64197185 | intron variant | C/T | snv | 0.39 | 2 | ||
| rs2715555 | 0.925 | 0.080 | 17 | 40388372 | downstream gene variant | G/A | snv | 9.5E-02 | 2 | ||
| rs761019455 | 1.000 | 0.080 | 15 | 81299818 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 | 1 | |
| rs7081735 | 1.000 | 0.080 | 10 | 127998792 | 5 prime UTR variant | G/A | snv | 0.72 | 1 | ||
| rs11650354 | 1.000 | 0.080 | 17 | 47744726 | intron variant | C/A;T | snv | 0.16 | 0.15 | 1 |