NM_001999.4(FBN2):c.7137T>G (p.Leu2379=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 26, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000604824.1
Allele description
NM_001999.4(FBN2):c.7137T>G (p.Leu2379=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2021