NM_153676.4(USH1C):c.2381-7_2381del AND Autosomal recessive nonsyndromic hearing loss 18A
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Sep 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003466497.1
Allele description [Variation Report for NM_153676.4(USH1C):c.2381-7_2381del]
NM_153676.4(USH1C):c.2381-7_2381del
Condition(s)
Assertion and evidence details
Last Updated: Dec 30, 2023