Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908188 | 0.742 | 0.360 | 1 | 25809753 | missense variant | G/A;C | snv | 1.8E-04 | 2 | ||
| rs121908182 | 1.000 | 0.120 | 1 | 25809096 | missense variant | G/A | snv | 1 | |||
| rs121908185 | 1.000 | 0.120 | 1 | 25813890 | missense variant | G/A | snv | 4.8E-05 | 6.3E-05 | 1 | |
| rs121908186 | 1.000 | 0.120 | 1 | 25812763 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs121908187 | 1.000 | 0.120 | 1 | 25812789 | missense variant | T/G | snv | 1 | |||
| rs749911126 | 1.000 | 0.120 | 1 | 25811462 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs756927098 | 1.000 | 0.120 | 1 | 25813898 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs776738184 | 1.000 | 0.120 | 1 | 25809688 | missense variant | A/G | snv | 8.0E-06 | 1 | ||
| rs779162837 | 1.000 | 0.120 | 1 | 25813899 | missense variant | G/A;T | snv | 1.6E-05; 4.0E-06 | 1 |