NM_178857.6(RP1L1):c.2791G>C (p.Gly931Arg) AND Occult macular 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:
- RCV000268558.5
Allele description [Variation Report for NM_178857.6(RP1L1):c.2791G>C (p.Gly931Arg)]
NM_178857.6(RP1L1):c.2791G>C (p.Gly931Arg)
Condition(s)
- Name:
- Occult macular dystrophy (OCMD)
- Synonyms:
- OMD; OCCULT MACULAR DYSTROPHY, SUSCEPTIBILITY TO
- Identifiers:
- MONDO: MONDO:0013316; MedGen: C3150833; Orphanet: 247834; OMIM: 613587; Human Phenotype Ontology: HP:0030636
Assertion and evidence details
Last Updated: Mar 16, 2024