Annotation Detail
Information
- Associated Genes
- IL2RA
- Associated Variants
-
NC_000010.11:g.6072697C>A
NC_000010.11:g.6072697C>A - Associated Disease
- IL2RA-related disorder
- Source Database
- ClinVar
- Description
- NC_000010.11:g.6072697C>A AND IL2RA-related disorder
- ClinVar Allele ID
- 29708
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2023-02-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003944824
- ClinVar Disease
- IL2RA-related disorder
- Observed Origin Sample
- germline
Drugs