RS55708915 ATP13A2

Health Risk Chr 1:16988161
Upload your DNA to see your genotype for this variant.
Associated Conditions
Kufor-Rakeb syndrome
Autosomal recessive spastic paraplegia type 78
Inborn genetic diseases
ATP13A2-related disorder
ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
Kufor-Rakeb syndrome
Autosomal recessive spastic paraplegia type 78
Inborn genetic diseases
ATP13A2-related disorder
ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
Other Variants in ATP13A2
rs786205056 rs2100817106 rs121918227 rs762033589 rs587776890 rs587777053 rs144701072 rs142616130 rs568367953 rs150519745
Ask Dr. Hemsworth about this variant