NM_001006658.3(CR2):c.2654G>A (p.Arg885His) AND Immunodeficiency, common variable, 7
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 25, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000650313.9
Allele description [Variation Report for NM_001006658.3(CR2):c.2654G>A (p.Arg885His)]
NM_001006658.3(CR2):c.2654G>A (p.Arg885His)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024