RS146170087 C19orf12
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neurodegeneration with brain iron accumulation 4
Dystonic disorder
Mental deterioration
Adult-onset night blindness
Peripheral visual field loss
Tremor
Hereditary spastic paraplegia 43
Hereditary spastic paraplegia 5A
Hereditary spastic paraplegia
Neurodegeneration with brain iron accumulation 4
Dystonic disorder
Mental deterioration
Adult-onset night blindness
Peripheral visual field loss
Tremor
Other Variants in C19orf12