RS121918165 LCA5
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What This Variant Does
"[OMIM:?]
Associated Conditions
Leber congenital amaurosis 5
Inborn genetic diseases
Retinal dystrophy
Leber congenital amaurosis
Leber congenital amaurosis 5
Inborn genetic diseases
Retinal dystrophy
Leber congenital amaurosis
Other Variants in LCA5