NM_000410.4(HFE):c.279G>C (p.Gly93=) AND Hereditary hemochromatosis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003590706.1
Allele description [Variation Report for NM_000410.4(HFE):c.279G>C (p.Gly93=)]
NM_000410.4(HFE):c.279G>C (p.Gly93=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024