NM_005121.3(MED13):c.5211C>G (p.Gly1737=) AND MED13-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 23, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003946559.1
Allele description
NM_005121.3(MED13):c.5211C>G (p.Gly1737=)
Condition(s)
- Name:
- MED13-related disorder
- Synonyms:
- MED13-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Aug 4, 2024