| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency +1 more | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency +2 more | |
| | CYP21A2, LOC106780800 (R103K +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
Click to view in NCBI Gene