RS770045008 TULP1

Health Risk Chr 6:35503626
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive retinitis pigmentosa
Retinal dystrophy
Leber congenital amaurosis
Retinitis pigmentosa 14
Leber congenital amaurosis 15
Autosomal recessive retinitis pigmentosa
Retinal dystrophy
Leber congenital amaurosis
Retinitis pigmentosa 14
Leber congenital amaurosis 15
Other Variants in TULP1
rs121909073 rs121909075 rs121909076 rs121909077 rs1581734819 rs1581742970 rs387906835 rs387906836 rs387906837 rs2150921548
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