RS797045412 BICD2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Spinal muscular atrophy
lower extremity-predominant
2
AD
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
2b
prenatal onset
autosomal dominant
Autosomal dominant hereditary axonal motor and sensory neuropathy
Inborn genetic diseases
Spinal muscular atrophy
lower extremity-predominant
2
AD
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Other Variants in BICD2