NM_001349338.3(FOXP1):c.*3391TG[10] AND Intellectual Disability with Language Impairment and Autistic Features
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000334331.6
Allele description [Variation Report for NM_001349338.3(FOXP1):c.*3391TG[10]]
NM_001349338.3(FOXP1):c.*3391TG[10]
Condition(s)
- Name:
- Intellectual Disability with Language Impairment and Autistic Features
- Identifiers:
- MedGen: CN239203
Assertion and evidence details
Last Updated: Apr 15, 2024