NM_000261.2(MYOC):c.573T>A (p.Thr191=) AND Glaucoma
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001102368.4
Allele description [Variation Report for NM_000261.2(MYOC):c.573T>A (p.Thr191=)]
NM_000261.2(MYOC):c.573T>A (p.Thr191=)
Condition(s)
- Name:
- Glaucoma
- Identifiers:
- MONDO: MONDO:0005041; MedGen: C0017601; Human Phenotype Ontology: HP:0000501
-
CHST9 [Hyaena hyaena]
CHST9 [Hyaena hyaena]Gene ID:120220443Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 13, 2023