RS398123031 BICD2

Health Risk Chr 9:92719122
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Hereditary spastic paraplegia 3A
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Hereditary spastic paraplegia 3A
Other Variants in BICD2
rs398123028 rs371707778 rs398123029 rs398123030 rs398123032 rs587777885 rs797044920 rs797045412 rs61754130 rs777986224
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