RS1064795760 BICD2

Health Risk Chr 9:92719007
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What This Variant Does
"CLNSIG=4
Associated Conditions
14 conditions
Spinal muscular atrophy
lower extremity-predominant
2b
prenatal onset
autosomal dominant
Inborn genetic diseases
14 conditions
Spinal muscular atrophy
lower extremity-predominant
2b
prenatal onset
autosomal dominant
Inborn genetic diseases
Other Variants in BICD2
rs398123028 rs371707778 rs398123029 rs398123030 rs398123031 rs398123032 rs587777885 rs797044920 rs797045412 rs61754130
Ask Dr. Hemsworth about this variant