NC_012920.1:m.7373A>G AND Optic atrophy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 21, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000408931.1
Allele description [Variation Report for NC_012920.1:m.7373A>G]
NC_012920.1:m.7373A>G
Condition(s)
- Name:
- Optic atrophy
- Identifiers:
- MONDO: MONDO:0003608; MedGen: C0029124; Human Phenotype Ontology: HP:0000648
Assertion and evidence details
Last Updated: May 24, 2022