NM_001493.3(GDI1):c.219T>C (p.Asn73=) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 12, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002312116.9
Allele description [Variation Report for NM_001493.3(GDI1):c.219T>C (p.Asn73=)]
NM_001493.3(GDI1):c.219T>C (p.Asn73=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024