NM_000397.4(CYBB):c.636T>C (p.Phe212=) AND Granulomatous disease, chronic, X-linked
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001460984.7
Allele description [Variation Report for NM_000397.4(CYBB):c.636T>C (p.Phe212=)]
NM_000397.4(CYBB):c.636T>C (p.Phe212=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024