| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FHAD1, LOC126805629 (Q122E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FHAD1, LOC126805629 (P128H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FHAD1, LOC126805629 (P143L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FHAD1, LOC126805629 (P160L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FHAD1, LOC126805629 (R165Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FHAD1, LOC126805629 (R182C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene