Variant: rs1064793745 

    present in Gene: LOC105372918;USH2A
    present in Chromosome: 1
    Position on Chromosome: 216199931
    Alleles of this Variant: C/T

rs1064793745 in LOC105372918;USH2A gene and RETINITIS PIGMENTOSA 39 (disorder) PMID 26969326 2016 Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss.

rs1064793745 in LOC105372918;USH2A gene and USHER SYNDROME, TYPE IIA PMID 26969326 2016 Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss.