NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 29, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000619724.9
Allele description [Variation Report for NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=)]
NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Apr 20, 2024