NM_003924.4(PHOX2B):c.430-19T>C AND Haddad syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003517521.1
Allele description [Variation Report for NM_003924.4(PHOX2B):c.430-19T>C]
NM_003924.4(PHOX2B):c.430-19T>C
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024