RS62638214 GRM6
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital stationary night blindness 1B
Retinal dystrophy
Leber congenital amaurosis
Congenital stationary night blindness 1B
Retinal dystrophy
Leber congenital amaurosis
Other Variants in GRM6