Variant: rs121918339 

    present in Gene: SLC17A8
    present in Chromosome: 12
    Position on Chromosome: 100396373
    Alleles of this Variant: C/T

rs121918339 in SLC17A8 gene and DEAFNESS, AUTOSOMAL DOMINANT 25 (disorder) PMID 18674745 2008 Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice.