NM_207352.4(CYP4V2):c.*2106G>T AND Corneal dystrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000338240.5
Allele description [Variation Report for NM_207352.4(CYP4V2):c.*2106G>T]
NM_207352.4(CYP4V2):c.*2106G>T
Condition(s)
- Name:
- Corneal dystrophy
- Identifiers:
- MONDO: MONDO:0018102; MedGen: C0010036; Human Phenotype Ontology: HP:0001131
Assertion and evidence details
Last Updated: Dec 24, 2023