Annotation Detail
Information
- Associated Genes
- UFD1
- Associated Variants
-
NC_000022.11:g.19479363T>C
NC_000022.11:g.19479363T>C - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NC_000022.11:g.19479363T>C AND not provided
- ClinVar Allele ID
- 1173442
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-05-17
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001539918
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs