NM_000552.5(VWF):c.2365A>G (p.Thr789Ala) AND von Willebrand disease type 1
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002243964.9
Allele description [Variation Report for NM_000552.5(VWF):c.2365A>G (p.Thr789Ala)]
NM_000552.5(VWF):c.2365A>G (p.Thr789Ala)
Condition(s)
Assertion and evidence details
Last Updated: May 26, 2024