| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ACBD4, LOC130061004 +1 more (R11C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ACBD4, LOC130061004 +1 more (A19V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene