Variant: rs549095193 

    present in Gene: TRIOBP
    present in Chromosome: 22
    Position on Chromosome: 37725611
    Alleles of this Variant: G/A;T

rs549095193 in TRIOBP gene and Deafness, Autosomal Recessive 28 PMID 16385457 2006 Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.

PMID 16385458 2006 Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.