Annotation Detail
Information
- Associated Genes
- FGG
- Associated Variants
-
FGG c.*216C>T
FGG c.*216C>T - Associated Disease
- congenital afibrinogenemia
- Source Database
- ClinVar
- Description
- NM_000509.5(FGG):c.*216C>T AND Congenital afibrinogenemia
- ClinVar Allele ID
- 353667
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2016-06-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000361528
- ClinVar Disease
- Congenital afibrinogenemia
- Observed Origin Sample
- germline
Drugs