NM_000518.5(HBB):c.9T>C (p.His3=) AND beta Thalassemia
- Germline classification:
- Benign (5 submissions)
- Last evaluated:
- Jul 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000328523.19
Allele description [Variation Report for NM_000518.5(HBB):c.9T>C (p.His3=)]
NM_000518.5(HBB):c.9T>C (p.His3=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024