RS1057518287 DYNC1H1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Intellectual disability
autosomal dominant 13
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Charcot-Marie-Tooth disease axonal type 2O
Inborn genetic diseases
Intellectual disability
autosomal dominant 13
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Charcot-Marie-Tooth disease axonal type 2O
Inborn genetic diseases
Other Variants in DYNC1H1