NM_001103146.3(GIGYF2):c.532+5798T>C AND Leber congenital amaurosis 16
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000275494.5
Allele description [Variation Report for NM_001103146.3(GIGYF2):c.532+5798T>C]
NM_001103146.3(GIGYF2):c.532+5798T>C
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023