| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | HYDIN, LOC126862387 (F579S +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | HYDIN, LOC126862387 (H573Y +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene