Variant: rs794729665

present in Gene: DCDC2 present in Chromosome: 6 Position on Chromosome: 24178385 Alleles of this Variant: T/G

rs794729665 in DCDC2 gene and Nonsyndromic Deafness PMID 25601850 2015 A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation.