Variant: rs143797113 

    present in Gene: CLDN14;LOC105369301
    present in Chromosome: 21
    Position on Chromosome: 36461208
    Alleles of this Variant: G/A

rs143797113 in CLDN14;LOC105369301 gene and DEAFNESS, AUTOSOMAL RECESSIVE 29 PMID 27838790 2017 A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.

PMID 26969326 2016 Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss.