RS186266220 RPGRIP1
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Associated Conditions
Cone-rod dystrophy 13
Leber congenital amaurosis 6
RPGRIP1-related disorder
Inborn genetic diseases
Cone-rod dystrophy 13
Leber congenital amaurosis 6
RPGRIP1-related disorder
Inborn genetic diseases
Other Variants in RPGRIP1