NM_000138.5(FBN1):c.3590-8T>C AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 16, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000125005.2
Allele description [Variation Report for NM_000138.5(FBN1):c.3590-8T>C]
NM_000138.5(FBN1):c.3590-8T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 30, 2024