Annotation Detail
Information
- Associated Genes
- Associated Variants
-
NC_000016.10:g.56959412C>A
NC_000016.10:g.56959412C>A - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NC_000016.10:g.56959412C>A AND not provided
- ClinVar Allele ID
- 171889
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000190313
- ClinVar Disease
- not provided
- Observed Origin Sample
- not provided
Drugs