| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs165815 | 0.882 | 0.120 | 22 | 19971950 | missense variant | C/T | snv | 0.75 | 0.72 | 5 | |
| rs165849 | 1.000 | 0.040 | 22 | 19971146 | intron variant | G/A | snv | 0.55 | 2 | ||
| rs35219372 | 22 | 19971288 | synonymous variant | C/A;G;T | snv | 6.1E-06; 6.1E-06; 1.7E-02 | 1 | ||||
| rs5993890 | 22 | 19971306 | synonymous variant | G/A;C | snv | 6.7E-02; 1.2E-05 | 1 |