RS763226083 DCTN1
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Associated Conditions
Inborn genetic diseases
Amyotrophic lateral sclerosis type 1
Perry syndrome
Neuronopathy
distal hereditary motor
type 7B
Inborn genetic diseases
Amyotrophic lateral sclerosis type 1
Perry syndrome
Neuronopathy
distal hereditary motor
type 7B
Other Variants in DCTN1