rs73568059

This variant is located in the CEACAM16 gene.

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ClinVar annotation

Likely Benign★★★☆

5 submitters3 publications

not specified; not provided; Hearing loss, autosomal recessive 113;Autosomal dominant nonsyndromic hearing loss 4B

About CEACAM16

The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012]

View all CEACAM16 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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