| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs8193038 | 0.925 | 0.080 | 6 | 52186584 | intron variant | A/G | snv | 2.2E-02 | 2 | ||
| rs11466024 | 0.925 | 0.080 | 16 | 3249468 | missense variant | C/A;T | snv | 1.6E-05; 1.3E-02 | 2 | ||
| rs224224 | 0.925 | 0.080 | 16 | 3254654 | synonymous variant | T/A;C | snv | 1.7E-04; 0.44 | 2 | ||
| rs1219605554 | 1.000 | 0.040 | 1 | 247425505 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs550622769 | 1.000 | 0.040 | 12 | 6329578 | missense variant | G/A;C | snv | 4.5E-06; 9.0E-06 | 1 |