Variant: rs397514607 

    present in Gene: OTOG
    present in Chromosome: 11
    Position on Chromosome: 17612638
    Alleles of this Variant: C/T

rs397514607 in OTOG gene and DEAFNESS, AUTOSOMAL RECESSIVE 18B PMID 23122587 2012 Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment.