NM_006516.4(SLC2A1):c.318C>T (p.Ser106=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 4, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002320019.9
Allele description [Variation Report for NM_006516.4(SLC2A1):c.318C>T (p.Ser106=)]
NM_006516.4(SLC2A1):c.318C>T (p.Ser106=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Nov 24, 2024