NM_000552.5(VWF):c.7997C>T (p.Thr2666Met) AND VWF-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 19, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004547572.2
Allele description [Variation Report for NM_000552.5(VWF):c.7997C>T (p.Thr2666Met)]
NM_000552.5(VWF):c.7997C>T (p.Thr2666Met)
Condition(s)
- Name:
- VWF-related disorder
- Synonyms:
- VWF-related disorders; VWF-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Oct 13, 2024