| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC124500673, SNX32 (T212I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124500673, SNX32 (E216K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene