Annotation Detail
Information
- Associated Genes
- CYP11B2 LOC110673971
- Associated Variants
-
CYP11B2 c.-344T>C
CYP11B2 c.-344T>C - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000498.3(CYP11B2):c.-344T>C AND not provided
- ClinVar Allele ID
- 775445
- ClinVar RefSeq Alternation Syntax
- NM_000498.3:c.-344T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000937219
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs