NM_206933.4(USH2A):c.13811+2T>C AND multiple conditions
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Feb 14, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000672770.1
Allele description [Variation Report for NM_206933.4(USH2A):c.13811+2T>C]
NM_206933.4(USH2A):c.13811+2T>C
Condition(s)
Assertion and evidence details
Last Updated: Jun 10, 2023