NM_020297.4(ABCC9):c.2139T>C (p.Ser713=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002430490.2
Allele description [Variation Report for NM_020297.4(ABCC9):c.2139T>C (p.Ser713=)]
NM_020297.4(ABCC9):c.2139T>C (p.Ser713=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: May 1, 2024