NM_000552.5(VWF):c.3789G>A (p.Ser1263=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000247036.18
Allele description [Variation Report for NM_000552.5(VWF):c.3789G>A (p.Ser1263=)]
NM_000552.5(VWF):c.3789G>A (p.Ser1263=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2024