NM_000144.5(FXN):c.97T>C (p.Leu33=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 31, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002311260.9
Allele description [Variation Report for NM_000144.5(FXN):c.97T>C (p.Leu33=)]
NM_000144.5(FXN):c.97T>C (p.Leu33=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Jun 2, 2024