RS199863781 IGHMBP2
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Associated Conditions
Neuronopathy
distal hereditary motor
autosomal dominant
Autosomal recessive distal spinal muscular atrophy 1
Charcot-Marie-Tooth disease axonal type 2S
Inborn genetic diseases
Neuronopathy
distal hereditary motor
autosomal dominant
Autosomal recessive distal spinal muscular atrophy 1
Charcot-Marie-Tooth disease axonal type 2S
Inborn genetic diseases
Other Variants in IGHMBP2