NM_001372574.1(ATXN2):c.289-11del AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001700280.2
Allele description [Variation Report for NM_001372574.1(ATXN2):c.289-11del]
NM_001372574.1(ATXN2):c.289-11del
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 23, 2022