RS767024102 CYP2U1

Health Risk Chr 4:107947458
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 56
Spastic paraplegia
Inborn genetic diseases
CYP2U1-related disorder
Hereditary spastic paraplegia 56
Spastic paraplegia
Inborn genetic diseases
CYP2U1-related disorder
Other Variants in CYP2U1
rs397514513 rs397514514 rs2476952905 rs397514515 rs141431913 rs1057519146 rs766380148 rs143913941 rs147506864 rs761575210
Ask Dr. Hemsworth about this variant