NM_152443.3(RDH12):c.672C>T (p.Thr224=) AND Leber congenital amaurosis 13
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003498136.1
Allele description [Variation Report for NM_152443.3(RDH12):c.672C>T (p.Thr224=)]
NM_152443.3(RDH12):c.672C>T (p.Thr224=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024