| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Indel (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Biotinidase deficiency | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Biotinidase deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Biotinidase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Biotinidase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Biotinidase deficiency +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Biotinidase deficiency +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene