RS398122409 C19orf12
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neurodegeneration with brain iron accumulation 4
Neurodegeneration with brain iron accumulation
Neurofibromatosis
type 1
Hereditary spastic paraplegia 43
Hereditary spastic paraplegia
Hereditary spastic paraplegia 43
Neurodegeneration with brain iron accumulation 4
Hereditary spastic paraplegia 43
Neurodegeneration with brain iron accumulation 4
Neurodegeneration with brain iron accumulation
Neurofibromatosis
type 1
Hereditary spastic paraplegia 43
Hereditary spastic paraplegia
Other Variants in C19orf12