Variant: rs397518022 

    present in Gene: LOC102723833;USH2A
    present in Chromosome: 1
    Position on Chromosome: 216072887
    Alleles of this Variant: A/G

rs397518022 in LOC102723833;USH2A gene and RETINITIS PIGMENTOSA 39 (disorder) PMID 20507924 2010 Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.

PMID 18641288 2008 Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.

rs397518022 in LOC102723833;USH2A gene and Usher Syndrome PMID 18641288 2008 Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.

PMID 20507924 2010 Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.