NM_001384140.1(PCDH15):c.4671+1642T>C AND PCDH15-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 18, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004543400.1
Allele description [Variation Report for NM_001384140.1(PCDH15):c.4671+1642T>C]
NM_001384140.1(PCDH15):c.4671+1642T>C
Condition(s)
- Name:
- PCDH15-related disorder
- Synonyms:
- PCDH15-Related Disorders; PCDH15-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 29, 2024