| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 28 | ||
| rs9551963 | 0.851 | 0.160 | 13 | 30758410 | intron variant | A/C;T | snv | 6 | |||
| rs17222842 | 0.882 | 0.120 | 13 | 30765980 | downstream gene variant | G/A | snv | 6.1E-02 | 3 | ||
| rs1209143268 | 1.000 | 0.040 | 2 | 43877840 | missense variant | T/G | snv | 8.0E-06 | 1 |