Variant: rs121965084 

    present in Gene: MYO7A
    present in Chromosome: 11
    Position on Chromosome: 77162149
    Alleles of this Variant: A/G;T

rs121965084 in MYO7A gene and Deafness, Autosomal Dominant 11 PMID 15300860 2004 Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11).

PMID 15121790 2004 Modifier controls severity of a novel dominant low-frequency MyosinVIIA (MYO7A) auditory mutation.

PMID 9354784 1997 Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.

PMID 15221449 2004 Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).