NM_018718.3(CEP41):c.974-8C>T AND Joubert syndrome 15
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000971283.8
Allele description [Variation Report for NM_018718.3(CEP41):c.974-8C>T]
NM_018718.3(CEP41):c.974-8C>T
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024