RS200057343 DCTN1
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Associated Conditions
Amyotrophic lateral sclerosis type 1
Neuronopathy
distal hereditary motor
type 7B
Perry syndrome
Inborn genetic diseases
Amyotrophic lateral sclerosis type 1
Neuronopathy
distal hereditary motor
type 7B
Perry syndrome
Inborn genetic diseases
Other Variants in DCTN1