| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ANKRD52, LOC132090122 (A1067T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ANKRD52, LOC132090122 (A1043T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ANKRD52, LOC132090122 (A1041V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene