NM_000410.4(HFE):c.636G>C (p.Val212=) AND Hereditary hemochromatosis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001470956.15
Allele description [Variation Report for NM_000410.4(HFE):c.636G>C (p.Val212=)]
NM_000410.4(HFE):c.636G>C (p.Val212=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 3, 2024