Annotation Detail
Information
- Associated Genes
- VWF
- Associated Variants
-
VWF p.Pro812ArgfsTer31 (p.P812Rfs*31)
(
ENST00000261405.10 )
VWF p.Pro812ArgfsTer31 (p.P812Rfs*31) ( ENST00000261405.10 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000552.5(VWF):c.2435del (p.Pro812fs) AND not provided
- ClinVar Allele ID
- 15342
- ClinVar RefSeq Alternation Syntax
- NM_000552.5:c.2435del
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-03-09
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000086611
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- not provided
- Observed Origin Sample
- unknown
Drugs