| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ARAP3, LOC126807531 (L1152M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ARAP3, LOC126807531 (T1141A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene