NM_014588.6(VSX1):c.528G>A (p.Leu176=) AND Posterior polymorphous corneal dystrophy
- Germline classification:
- 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:
- RCV000362369.5
Allele description [Variation Report for NM_014588.6(VSX1):c.528G>A (p.Leu176=)]
NM_014588.6(VSX1):c.528G>A (p.Leu176=)
Condition(s)
- Name:
- Posterior polymorphous corneal dystrophy
- Synonyms:
- Polymorphous corneal dystrophy; CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR
- Identifiers:
- MONDO: MONDO:0020364; MedGen: C0339284; OMIM: PS122000; Human Phenotype Ontology: HP:0007915
-
Gm36246 predicted gene, 36246 [Mus musculus]
Gm36246 predicted gene, 36246 [Mus musculus]Gene ID:102640093Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Jul 15, 2024