Variant: rs121917828 

    present in Gene: CABP4
    present in Chromosome: 11
    Position on Chromosome: 67456191
    Alleles of this Variant: C/T

rs121917828 in CABP4 gene and Cone-rod synaptic disorder, congenital nonprogressive PMID 16960802 2006 Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.