NM_000410.4(HFE):c.492C>T (p.Pro164=) AND Hereditary hemochromatosis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003590768.1
Allele description [Variation Report for NM_000410.4(HFE):c.492C>T (p.Pro164=)]
NM_000410.4(HFE):c.492C>T (p.Pro164=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024