NM_001195794.1(CLRN1):c.-141C>T AND Usher syndrome type 3
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001147610.13
Allele description [Variation Report for NM_001195794.1(CLRN1):c.-141C>T]
NM_001195794.1(CLRN1):c.-141C>T
Condition(s)
- Name:
- Usher syndrome type 3
- Synonyms:
- Usher Syndrome, Type III
- Identifiers:
- MONDO: MONDO:0016485; MedGen: C1568248
Assertion and evidence details
Last Updated: Jul 29, 2024