RS917027829 CSF1R
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Associated Conditions
Inborn genetic diseases
Brain abnormalities
neurodegeneration
and dysosteosclerosis
Hereditary diffuse leukoencephalopathy with spheroids
Inborn genetic diseases
Brain abnormalities
neurodegeneration
and dysosteosclerosis
Hereditary diffuse leukoencephalopathy with spheroids
Other Variants in CSF1R