| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | AEBP2, LOC130007517 (E44A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | AEBP2, LOC130007517 (E45G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | AEBP2, LOC130007517 (G66D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene