| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ACADVL, LOC130060113 (S22W +1 more) | Single nucleotide variant (missense variant +1 more) | Very long chain acyl-CoA dehydrogenase deficiency | |
| | ACADVL, LOC130060113 (R23Q +1 more) | Single nucleotide variant (missense variant +1 more) | Very long chain acyl-CoA dehydrogenase deficiency | |
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