Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2235371 | 0.752 | 0.360 | 1 | 209790735 | missense variant | C/T | snv | 8.7E-02 | 3.9E-02 | 11 | |
| rs2235375 | 0.807 | 0.400 | 1 | 209792242 | intron variant | G/A;C;T | snv | 3.2E-05; 0.41; 4.3E-04 | 7 | ||
| rs2013162 | 0.827 | 0.280 | 1 | 209795339 | synonymous variant | C/A;T | snv | 0.41; 1.6E-05 | 5 | ||
| rs28942094 | 0.851 | 0.400 | 1 | 209801398 | missense variant | G/A | snv | 4 |