Variant: rs121908969 

    present in Gene: MYO15A;LOC105371566;LOC105371567
    present in Chromosome: 17
    Position on Chromosome: 18154190
    Alleles of this Variant: G/T

rs121908969 in MYO15A;LOC105371566;LOC105371567 gene and Deafness, Autosomal Recessive 3 PMID 24926664 2014 Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.

PMID 11735029 2001 Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.

PMID 9603736 1998 Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.