Variant: rs35689081 

    present in Gene: MYO7A
    present in Chromosome: 11
    Position on Chromosome: 77142783
    Alleles of this Variant: C/A;T

rs35689081 in MYO7A gene and DEAFNESS, AUTOSOMAL RECESSIVE 2 PMID 10094549 1999 Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity.

PMID 19074810 2009 Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.

rs35689081 in MYO7A gene and Retinitis Pigmentosa PMID 30718709 2019 Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.

rs35689081 in MYO7A gene and Usher Syndrome, Type I PMID 10094549 1999 Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity.

PMID 19074810 2009 Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.