NM_018249.6(CDK5RAP2):c.5308-6G>T AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002548329.2
Allele description [Variation Report for NM_018249.6(CDK5RAP2):c.5308-6G>T]
NM_018249.6(CDK5RAP2):c.5308-6G>T
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 20, 2024