NM_001453.3(FOXC1):c.628G>A (p.Asp210Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002804329.2
Allele description [Variation Report for NM_001453.3(FOXC1):c.628G>A (p.Asp210Asn)]
NM_001453.3(FOXC1):c.628G>A (p.Asp210Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024