RS121909075 TULP1

Health Risk Chr 6:35500100
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Retinitis pigmentosa 14
Leber congenital amaurosis
Retinal dystrophy
TULP1-related disorder
Retinitis pigmentosa 14
Retinitis pigmentosa 14
Leber congenital amaurosis
Retinal dystrophy
TULP1-related disorder
Retinitis pigmentosa 14
Other Variants in TULP1
rs121909073 rs121909076 rs121909077 rs1581734819 rs1581742970 rs387906835 rs387906836 rs387906837 rs2150921548 rs62636511
Ask Dr. Hemsworth about this variant