| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | Deficiency of 3-hydroxyacyl-CoA dehydrogenase +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene