Variant: rs111033267 

    present in Gene: CLRN1;CLRN1-AS1
    present in Chromosome: 3
    Position on Chromosome: 150972520
    Alleles of this Variant: G/A;T

rs111033267 in CLRN1;CLRN1-AS1 gene and Retinitis Pigmentosa PMID 12080385 2002 USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses.

rs111033267 in CLRN1;CLRN1-AS1 gene and Usher Syndrome, Type III PMID 24596593 2014 Strategies for genetic study of hearing loss in the Brazilian northeastern region.

PMID 12080385 2002 USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses.

PMID 23304067 2012 Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.