NM_015058.2(VWA8):c.1552C>T (p.Arg518Trp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004104107.1
Allele description [Variation Report for NM_015058.2(VWA8):c.1552C>T (p.Arg518Trp)]
NM_015058.2(VWA8):c.1552C>T (p.Arg518Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 16, 2024