RS139402633 TULP1

Health Risk Chr 6:35503792
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Associated Conditions
Retinitis pigmentosa
Leber congenital amaurosis 15
Inborn genetic diseases
Retinitis pigmentosa
Leber congenital amaurosis 15
Inborn genetic diseases
Other Variants in TULP1
rs121909073 rs121909075 rs121909076 rs121909077 rs1581734819 rs1581742970 rs387906835 rs387906836 rs387906837 rs2150921548
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