| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ACADVL, LOC130060113 (R37W +1 more) | Single nucleotide variant (missense variant +1 more) | Very long chain acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (synonymous variant +1 more) | Very long chain acyl-CoA dehydrogenase deficiency | |
| | ACADVL, LOC130060113 (A67T +1 more) | Single nucleotide variant (missense variant +1 more) | Very long chain acyl-CoA dehydrogenase deficiency +1 more | |
Click to view in NCBI Gene