| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified +2 more | |
| | CYP21A2, LOC106780800 (L176P +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | CYP21A2, LOC106780800 (V282L +2 more) | Single nucleotide variant (missense variant) | CYP21A2-related condition +4 more | GPathogenic/Likely pathogenic |
| | CYP21A2, LOC106780800 +1 more | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | CYP21A2, LOC106780800 +1 more | Single nucleotide variant (intron variant) | not provided | |
| | CYP21A2, LOC106780800 +1 more | Single nucleotide variant (intron variant) | not provided | |
| | CYP21A2, LOC106780800 +1 more | Single nucleotide variant (intron variant) | not provided | |
| | CYP21A2, LOC106780800 +1 more (R480L +2 more) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
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