RS374912668 BICD2

Health Risk Chr 9:92718986
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Inborn genetic diseases
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures
Inborn genetic diseases
Other Variants in BICD2
rs398123028 rs371707778 rs398123029 rs398123030 rs398123031 rs398123032 rs587777885 rs797044920 rs797045412 rs61754130
Ask Dr. Hemsworth about this variant