RS794727634 DYNC1H1
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Associated Conditions
Charcot-Marie-Tooth disease axonal type 2O
Inborn genetic diseases
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Peripheral neuropathy
See cases
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease axonal type 2O
Inborn genetic diseases
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Peripheral neuropathy
See cases
Charcot-Marie-Tooth disease
Other Variants in DYNC1H1