NM_000141.5(FGFR2):c.454+14C>T AND Isolated coronal synostosis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001105636.5
Allele description [Variation Report for NM_000141.5(FGFR2):c.454+14C>T]
NM_000141.5(FGFR2):c.454+14C>T
Condition(s)
- Name:
- Isolated coronal synostosis
- Identifiers:
- MedGen: CN043619
Assertion and evidence details
Last Updated: Sep 29, 2024