NM_001159699.2(FHL1):c.132C>T (p.Cys44=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004373960.1
Allele description [Variation Report for NM_001159699.2(FHL1):c.132C>T (p.Cys44=)]
NM_001159699.2(FHL1):c.132C>T (p.Cys44=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Sep 29, 2024