NM_207352.4(CYP4V2):c.64C>G (p.Leu22Val) AND Corneal dystrophy
- Germline classification:
- 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:
- RCV000278726.13
Allele description [Variation Report for NM_207352.4(CYP4V2):c.64C>G (p.Leu22Val)]
NM_207352.4(CYP4V2):c.64C>G (p.Leu22Val)
Condition(s)
- Name:
- Corneal dystrophy
- Identifiers:
- MONDO: MONDO:0018102; MedGen: C0010036; Human Phenotype Ontology: HP:0001131
Assertion and evidence details
Last Updated: Apr 15, 2024