Variant: rs121908449 

    present in Gene: RGS9
    present in Chromosome: 17
    Position on Chromosome: 65197160
    Alleles of this Variant: T/C

rs121908449 in RGS9 gene and Leber Congenital Amaurosis PMID 30718709 2019 Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.

rs121908449 in RGS9 gene and Prolonged Electroretinal Response Suppression PMID 14702087 2004 Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation.