NM_000531.6(OTC):c.298+5G>C AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 9, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002313837.9
Allele description [Variation Report for NM_000531.6(OTC):c.298+5G>C]
NM_000531.6(OTC):c.298+5G>C
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Aug 18, 2024