Variant: rs1562505728 

    present in Gene: EYA4;TARID
    present in Chromosome: 6
    Position on Chromosome: 133512884
    Alleles of this Variant: C/G

rs1562505728 in EYA4;TARID gene and Deafness, Autosomal Dominant 10 PMID 15735644 2005 Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.

PMID 11159937 2001 Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.

PMID 17567890 2007 Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.

PMID 25781927 2015 Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss.