Annotation Detail
Information
- Associated Genes
- VWF
- Associated Variants
-
VWF c.-1303G>A
VWF c.-1303G>A - Associated Disease
- VWF-related disorder
- Source Database
- ClinVar
- Description
- NM_000552.3(VWF):c.-1303G>A AND VWF-related disorder
- ClinVar Allele ID
- 611318
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2019-03-05
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004547951
- ClinVar Disease
- VWF-related disorder
- Observed Origin Sample
- germline
Drugs