NM_206933.4(USH2A):c.848+5G>C AND Retinitis pigmentosa 39
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003445130.1
Allele description [Variation Report for NM_206933.4(USH2A):c.848+5G>C]
NM_206933.4(USH2A):c.848+5G>C
Condition(s)
Assertion and evidence details
Last Updated: Oct 20, 2024