NM_000138.5(FBN1):c.4211-10C>T AND FBN1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004537904.1
Allele description [Variation Report for NM_000138.5(FBN1):c.4211-10C>T]
NM_000138.5(FBN1):c.4211-10C>T
Condition(s)
- Name:
- FBN1-related disorder
- Identifiers:
Assertion and evidence details
Last Updated: Sep 29, 2024