Variant: rs62638197 

    present in Gene: GRM6
    present in Chromosome: 5
    Position on Chromosome: 178994808
    Alleles of this Variant: G/A

rs62638197 in GRM6 gene and Night blindness, congenital stationary PMID 16249515 2005 Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.