NM_003896.4(ST3GAL5):c.662+13T>C AND GM3 synthase deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003613725.2
Allele description [Variation Report for NM_003896.4(ST3GAL5):c.662+13T>C]
NM_003896.4(ST3GAL5):c.662+13T>C
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024