NM_000552.5(VWF):c.7682T>A (p.Phe2561Tyr) AND Hereditary von Willebrand disease
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000368572.6
Allele description [Variation Report for NM_000552.5(VWF):c.7682T>A (p.Phe2561Tyr)]
NM_000552.5(VWF):c.7682T>A (p.Phe2561Tyr)
Condition(s)
- Name:
- Hereditary von Willebrand disease
- Identifiers:
- MONDO: MONDO:0019565; MeSH: D014842; MedGen: C5703318
Assertion and evidence details
Last Updated: May 12, 2024