Annotation Detail
Information
- Associated Genes
- CYP21A2 LOC106780800
- Associated Variants
-
CYP21A2 p.Val282Leu (p.V282L)
(
ENST00000435122.3,
ENST00000644719.2 )
CYP21A2 p.Val282Leu (p.V282L) ( ENST00000435122.3, ENST00000644719.2 ) - Associated Disease
- congenital adrenal hyperplasia
- Source Database
- ClinVar
- Description
- NM_000500.9(CYP21A2):c.844G>T (p.Val282Leu) AND Congenital adrenal hyperplasia
- ClinVar Allele ID
- 27190
- ClinVar RefSeq Alternation Syntax
- NM_001368143.2:c.439G>T
- ClinVar RefSeq Alternation Syntax
- NM_000500.9:c.844G>T
- ClinVar RefSeq Alternation Syntax
- NM_001128590.4:c.754G>T
- ClinVar RefSeq Alternation Syntax
- NM_001368144.2:c.439G>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-12-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001804725
- ClinVar Disease
- Congenital adrenal hyperplasia
- Observed Origin Sample
- germline
Drugs