NM_000261.2(MYOC):c.*182C>A AND Glaucoma
- 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:
- RCV000285690.5
Allele description [Variation Report for NM_000261.2(MYOC):c.*182C>A]
NM_000261.2(MYOC):c.*182C>A
Condition(s)
- Name:
- Glaucoma
- Identifiers:
- MONDO: MONDO:0005041; MedGen: C0017601; Human Phenotype Ontology: HP:0000501
Assertion and evidence details
Last Updated: Apr 9, 2023