Annotation Detail
Information
- Associated Genes
- NFKBIA
- Associated Variants
-
NC_000014.9:g.35405064G>A
NC_000014.9:g.35405064G>A - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NC_000014.9:g.35405064G>A AND not provided
- ClinVar Allele ID
- 1157242
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-06-19
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001655765
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs