RS61754130 BICD2
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Associated Conditions
Hereditary spastic paraplegia
Neuronopathy
distal hereditary motor
autosomal dominant
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Inborn genetic diseases
BICD2-related disorder
Hereditary spastic paraplegia
Neuronopathy
distal hereditary motor
autosomal dominant
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Inborn genetic diseases
BICD2-related disorder
Other Variants in BICD2