| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CYP17A1, CYP17A1-AS1 (N290fs) | Deletion (frameshift variant) | Deficiency of steroid 17-alpha-monooxygenase +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Deficiency of steroid 17-alpha-monooxygenase +1 more | |
| | | Single nucleotide variant (synonymous variant) | Deficiency of steroid 17-alpha-monooxygenase +1 more | |
| | CYP17A1, CYP17A1-AS1 (F224S) | Single nucleotide variant (missense variant) | Deficiency of steroid 17-alpha-monooxygenase | |
Click to view in NCBI Gene