| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Microsatellite (frameshift variant) | Myopathy with abnormal lipid metabolism +1 more | |
| | | Indel (frameshift variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Duplication (frameshift variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Deletion (frameshift variant) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Deletion (inframe_deletion) | Multiple acyl-CoA dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Multiple acyl-CoA dehydrogenase deficiency +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene