NM_006516.4(SLC2A1):c.498C>T (p.Val166=) AND History of neurodevelopmental disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 17, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000717977.1
Allele description
NM_006516.4(SLC2A1):c.498C>T (p.Val166=)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
Assertion and evidence details
Last Updated: Oct 22, 2022