| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion | Deficiency of 3-hydroxyacyl-CoA dehydrogenase +3 more | GUncertain significance/Uncertain risk allele |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Deficiency of 3-hydroxyacyl-CoA dehydrogenase +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Deficiency of 3-hydroxyacyl-CoA dehydrogenase +5 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene