Variant: rs104894115 

    present in Gene: PUM3;KCNV2
    present in Chromosome: 9
    Position on Chromosome: 2729465
    Alleles of this Variant: G/A

rs104894115 in PUM3;KCNV2 gene and Retinal Cone Dystrophy 3B PMID 16909397 2006 "Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause ""cone dystrophy with supernormal rod electroretinogram"" in humans."