Variant: rs746551311 

    present in Gene: LOC105372918;USH2A
    present in Chromosome: 1
    Position on Chromosome: 216196582
    Alleles of this Variant: G/A

rs746551311 in LOC105372918;USH2A gene and RETINITIS PIGMENTOSA 39 (disorder) PMID 26856745 2016 Next-generation sequencing-based molecular diagnosis of 12 inherited retinal disease probands of Uyghur ethnicity.

PMID 27460420 2016 An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.

PMID 15325563 2004 Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.

rs746551311 in LOC105372918;USH2A gene and Retinitis Pigmentosa PMID 15325563 2004 Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.

rs746551311 in LOC105372918;USH2A gene and USHER SYNDROME, TYPE IIA PMID 27460420 2016 An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.

PMID 26856745 2016 Next-generation sequencing-based molecular diagnosis of 12 inherited retinal disease probands of Uyghur ethnicity.

PMID 15325563 2004 Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.