Variant: rs1555543296 

    present in Gene: MYO15A;LOC105371566
    present in Chromosome: 17
    Position on Chromosome: 18135775
    Alleles of this Variant: T/G

rs1555543296 in MYO15A;LOC105371566 gene and Multiple congenital anomalies PMID 25792667 2015 Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis.

PMID 7704031 1995 A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

PMID 7616538 1995 Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village.

PMID 18804553 2009 Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

PMID 26242193 2015 Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing.

PMID 27375115 2016 Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.