RS1367809298 BICD2

Health Risk Chr 9:92720601
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Associated Conditions
Hereditary spastic paraplegia
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Hereditary spastic paraplegia
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Other Variants in BICD2
rs398123028 rs371707778 rs398123029 rs398123030 rs398123031 rs398123032 rs587777885 rs797044920 rs797045412 rs61754130
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