| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130066506, RWDD2B (S6F) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC130066506, RWDD2B (I3T) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene