RS62637015 AIPL1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Leber congenital amaurosis 4
Leber congenital amaurosis 1
AIPL1-related disorder
Myopia 25
autosomal dominant
Nystagmus
High myopia
early-onset
Leber congenital amaurosis 4
Leber congenital amaurosis 1
AIPL1-related disorder
Myopia 25
autosomal dominant
Nystagmus
High myopia
Other Variants in AIPL1