RS916661191 BICD2

Health Risk Chr 9:92718958
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Associated Conditions
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Neuronopathy
distal hereditary motor
type 5B
Inborn genetic diseases
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Neuronopathy
distal hereditary motor
type 5B
Inborn genetic diseases
Other Variants in BICD2
rs398123028 rs371707778 rs398123029 rs398123030 rs398123031 rs398123032 rs587777885 rs797044920 rs797045412 rs61754130
Ask Dr. Hemsworth about this variant