RS766196673 CYP2U1

Health Risk Chr 4:107944993
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Associated Conditions
Inborn genetic diseases
Spastic paraplegia
Inborn genetic diseases
Spastic paraplegia
Other Variants in CYP2U1
rs397514513 rs397514514 rs2476952905 rs397514515 rs141431913 rs1057519146 rs766380148 rs143913941 rs147506864 rs767024102
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