Variant: rs104894395 

    present in Gene: GJB2
    present in Chromosome: 13
    Position on Chromosome: 20189352
    Alleles of this Variant: C/T

rs104894395 in GJB2 gene and DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder) PMID 22695344 2012 The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.

PMID 12792423 2003 Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness.

PMID 19707039 2009 High prevalence of the connexin 26 (GJB2) mutation in Chinese cochlear implant recipients.