Annotation Detail
Information
- Associated Genes
- Associated Variants
-
NC_000023.11:g.136644791A>G
NC_000023.11:g.136644791A>G - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NC_000023.11:g.136644791A>G AND not provided
- ClinVar Allele ID
- 800210
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2022-09-13
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001811567
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs