Variant: rs876661405 

    present in Gene: LOC107985305;CEACAM16
    present in Chromosome: 19
    Position on Chromosome: 44704140
    Alleles of this Variant: G/A

rs876661405 in LOC107985305;CEACAM16 gene and DEAFNESS, AUTOSOMAL DOMINANT 4B PMID 25589040 2015 Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.

PMID 21368133 2011 Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).