NM_000203.5(IDUA):c.558C>T (p.His186=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003169348.2
Allele description [Variation Report for NM_000203.5(IDUA):c.558C>T (p.His186=)]
NM_000203.5(IDUA):c.558C>T (p.His186=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024