Variant: rs786205121 

    present in Gene: KCNV2
    present in Chromosome: 9
    Position on Chromosome: 2717745
    Alleles of this Variant: AACA/-

rs786205121 in KCNV2 gene and Retinal Dystrophies PMID 21882291 2011 Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.