NM_003227.4(TFR2):c.2277C>T (p.Pro759=) AND Hereditary hemochromatosis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001458253.6
Allele description [Variation Report for NM_003227.4(TFR2):c.2277C>T (p.Pro759=)]
NM_003227.4(TFR2):c.2277C>T (p.Pro759=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024