NM_015046.7(SETX):c.5781+12dup AND Ataxia with Oculomotor Apraxia
- Germline classification:
- Benign (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:
- RCV000370219.3
Allele description
NM_015046.7(SETX):c.5781+12dup
Condition(s)
- Name:
- Ataxia with Oculomotor Apraxia
- Identifiers:
- MedGen: CN239198
Assertion and evidence details
Last Updated: Feb 20, 2022