NM_207361.6(FREM2):c.2987T>A (p.Val996Asp) AND FREM2-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003408027.4
Allele description [Variation Report for NM_207361.6(FREM2):c.2987T>A (p.Val996Asp)]
NM_207361.6(FREM2):c.2987T>A (p.Val996Asp)
Condition(s)
- Name:
- FREM2-related disorder
- Synonyms:
- FREM2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 12, 2024