RS397514513 CYP2U1

Health Risk Chr 4:107945426
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 56
Neurodegeneration
Global developmental delay
Spastic paraplegia
CYP2U1-related disorder
Hereditary spastic paraplegia 56
Neurodegeneration
Global developmental delay
Spastic paraplegia
CYP2U1-related disorder
Other Variants in CYP2U1
rs397514514 rs2476952905 rs397514515 rs141431913 rs1057519146 rs766380148 rs143913941 rs147506864 rs767024102 rs761575210
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