RS780594709 IGHMBP2

Health Risk Chr 11:68933854
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease axonal type 2S
Autosomal recessive distal spinal muscular atrophy 1
Neuronopathy
distal hereditary motor
autosomal dominant
Inborn genetic diseases
Charcot-Marie-Tooth disease axonal type 2S
Autosomal recessive distal spinal muscular atrophy 1
Neuronopathy
distal hereditary motor
autosomal dominant
Inborn genetic diseases
Other Variants in IGHMBP2
rs137852665 rs137852666 rs137852667 rs137852668 rs786205089 rs137852669 rs786205090 rs137852670 rs372000714 rs724159994
Ask Dr. Hemsworth about this variant