Annotation Detail
Information
- Associated Genes
- VWF
- Associated Variants
-
VWF c.-1303G>A
VWF c.-1303G>A - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000552.3(VWF):c.-1303G>A AND not provided
- ClinVar Allele ID
- 611318
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-04-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000760108
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs