Annotation Detail
Information
- Associated Genes
- CCDC170
- Associated Variants
-
NC_000006.12:g.151627231G>A
NC_000006.12:g.151627231G>A - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NC_000006.12:g.151627231G>A AND not specified
- ClinVar Allele ID
- 165626
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2020-10-28
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001777152
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs