Annotation Detail
Information
- Associated Genes
- CYP21A2 LOC106780800
- Associated Variants
-
CYP21A2 c.293-13C>G
(
ENST00000435122.3,
ENST00000644719.2 )
CYP21A2 c.293-13C>G ( ENST00000435122.3, ENST00000644719.2 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000500.9(CYP21A2):c.293-13C>G AND Inborn genetic diseases
- ClinVar Allele ID
- 27194
- ClinVar RefSeq Alternation Syntax
- NM_001368144.2:c.-126C>G
- ClinVar RefSeq Alternation Syntax
- NM_000500.9:c.293-13C>G
- ClinVar RefSeq Alternation Syntax
- NM_001128590.4:c.203-13C>G
- ClinVar RefSeq Alternation Syntax
- NM_001368143.2:c.-126C>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2016-04-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000624227
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs