RS140841480 DYNC1H1
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Associated Conditions
Intellectual disability
autosomal dominant 13
Charcot-Marie-Tooth disease axonal type 2O
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Autosomal dominant cerebellar ataxia
Charcot-Marie-Tooth disease
Inborn genetic diseases
DYNC1H1-related disorder
Intellectual disability
autosomal dominant 13
Charcot-Marie-Tooth disease axonal type 2O
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Autosomal dominant cerebellar ataxia
Charcot-Marie-Tooth disease
Inborn genetic diseases
Other Variants in DYNC1H1