RS765632065 ATP13A2
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Associated Conditions
Kufor-Rakeb syndrome
Autosomal recessive spastic paraplegia type 78
Neurodegeneration with brain iron accumulation
Inborn genetic diseases
Kufor-Rakeb syndrome
Autosomal recessive spastic paraplegia type 78
Neurodegeneration with brain iron accumulation
Inborn genetic diseases
Other Variants in ATP13A2