NM_000552.5(VWF):c.5222T>C (p.Ile1741Thr) AND von Willebrand disease type 1
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003313833.2
Allele description [Variation Report for NM_000552.5(VWF):c.5222T>C (p.Ile1741Thr)]
NM_000552.5(VWF):c.5222T>C (p.Ile1741Thr)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024