| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | ACACA, LOC126862545 (N2156S +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | ACACA, LOC126862545 (T2210S +3 more) | Single nucleotide variant (missense variant) | not provided | |
Click to view in NCBI Gene