NM_207352.4(CYP4V2):c.*1986G>A AND Corneal dystrophy
- Germline classification:
- Uncertain significance (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:
- RCV001149318.4
Allele description [Variation Report for NM_207352.4(CYP4V2):c.*1986G>A]
NM_207352.4(CYP4V2):c.*1986G>A
Condition(s)
- Name:
- Corneal dystrophy
- Identifiers:
- MONDO: MONDO:0018102; MedGen: C0010036; Human Phenotype Ontology: HP:0001131
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Last Updated: Dec 24, 2023