NM_000261.2(MYOC):c.1188G>A (p.Glu396=) AND Glaucoma
- Germline classification:
- Likely benign (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:
- RCV000337368.6
Allele description [Variation Report for NM_000261.2(MYOC):c.1188G>A (p.Glu396=)]
NM_000261.2(MYOC):c.1188G>A (p.Glu396=)
Condition(s)
- Name:
- Glaucoma
- Identifiers:
- MONDO: MONDO:0005041; MedGen: C0017601; Human Phenotype Ontology: HP:0000501
Assertion and evidence details
Last Updated: Sep 29, 2024