NM_014285.7(EXOSC2):c.673-1G>T AND Neurodevelopmental delay
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 17, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000761615.1
Allele description [Variation Report for NM_014285.7(EXOSC2):c.673-1G>T]
NM_014285.7(EXOSC2):c.673-1G>T
Condition(s)
- Name:
- Neurodevelopmental delay
- Identifiers:
- MedGen: C4022738; Human Phenotype Ontology: HP:0012758
Assertion and evidence details
Last Updated: Apr 6, 2024