RS772567265 TUBGCP6

Health Risk Chr 22:50220490
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Associated Conditions
Inborn genetic diseases
Retinal dystrophy
Inborn genetic diseases
Retinal dystrophy
Other Variants in TUBGCP6
rs387907019 rs727502807 rs724159975 rs724159976 rs724159997 rs201721812 rs772174079 rs781746721 rs141805017 rs192919234
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