NM_178335.3(CCDC50):c.976+56A>G AND Autosomal dominant nonsyndromic hearing loss 44
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001554847.2
Allele description [Variation Report for NM_178335.3(CCDC50):c.976+56A>G]
NM_178335.3(CCDC50):c.976+56A>G
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023