NM_000405.5(GM2A):c.*1239dup AND Tay-Sachs disease, variant AB
- 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:
- RCV000347139.5
Allele description [Variation Report for NM_000405.5(GM2A):c.*1239dup]
NM_000405.5(GM2A):c.*1239dup
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023