NM_153676.4(USH1C):c.1086-45A>G AND Autosomal recessive nonsyndromic hearing loss 18A
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001538055.2
Allele description [Variation Report for NM_153676.4(USH1C):c.1086-45A>G]
NM_153676.4(USH1C):c.1086-45A>G
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023