NM_000141.5(FGFR2):c.109+7033T>C AND FGFR2-related craniosynostosis
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002181484.5
Allele description [Variation Report for NM_000141.5(FGFR2):c.109+7033T>C]
NM_000141.5(FGFR2):c.109+7033T>C
Condition(s)
- Name:
- FGFR2-related craniosynostosis
- Identifiers:
- MedGen: CN231480
Assertion and evidence details
Last Updated: Feb 20, 2024