| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FAHD1, LOC130058194 (L57I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAHD1, LOC130058194 (R63C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene