NM_000405.5(GM2A):c.182C>G (p.Pro61Arg) AND Tay-Sachs disease, variant AB
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003087830.2
Allele description [Variation Report for NM_000405.5(GM2A):c.182C>G (p.Pro61Arg)]
NM_000405.5(GM2A):c.182C>G (p.Pro61Arg)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024