| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1013940 | 0.827 | 0.160 | 2 | 107992192 | missense variant | A/G | snv | 9.3E-02 | 7.4E-02 | 6 | |
| rs80359890 | 0.851 | 0.080 | 5 | 149042718 | missense variant | A/G | snv | 1.6E-03; 4.0E-06 | 2.0E-03 | 4 | |
| rs116840817 | 0.925 | 0.080 | X | 71223852 | missense variant | T/C | snv | 3 | |||
| rs3784867 | 1.000 | 0.040 | 16 | 16109488 | intron variant | C/T | snv | 0.25 | 1 |