NM_152564.5(VPS13B):c.3082+13T>C AND Cohen syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003013292.3
Allele description [Variation Report for NM_152564.5(VPS13B):c.3082+13T>C]
NM_152564.5(VPS13B):c.3082+13T>C
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024