Annotation Detail
Information
- Associated Genes
- MRE11
- Associated Variants
-
NC_000011.10:g.94493959C>A
NC_000011.10:g.94493959C>A - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NC_000011.10:g.94493959C>A AND not provided
- ClinVar Allele ID
- 1280899
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-06-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001716768
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs