RS752450983 C19orf12
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What This Variant Does
"CLNSIG=4
Associated Conditions
Global developmental delay
Intellectual disability
Neurodegeneration with brain iron accumulation 4
Neurodegeneration with brain iron accumulation 4
Hereditary spastic paraplegia 43
Neurodegeneration with brain iron accumulation
Global developmental delay
Intellectual disability
Neurodegeneration with brain iron accumulation 4
Neurodegeneration with brain iron accumulation 4
Hereditary spastic paraplegia 43
Neurodegeneration with brain iron accumulation
Other Variants in C19orf12