| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CYP21A2, LOC106780800 (A392T +2 more) | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | CYP21A2, LOC106780800 (P454S +2 more) | Single nucleotide variant (missense variant) | CYP21A2-related disorder +4 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene