Variant: rs121912560 

    present in Gene: MYO6
    present in Chromosome: 6
    Position on Chromosome: 75841299
    Alleles of this Variant: A/G

rs121912560 in MYO6 gene and Deafness, autosomal dominant nonsyndromic sensorineural 22 PMID 15060111 2004 Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6).