RS35092963 DYNC1H1

Health Risk Chr 14:101986601
Upload your DNA to see your genotype for this variant.
Associated Conditions
Charcot-Marie-Tooth disease axonal type 2O
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Intellectual disability
autosomal dominant 13
Autosomal dominant cerebellar ataxia
Inborn genetic diseases
DYNC1H1-related disorder
Charcot-Marie-Tooth disease axonal type 2O
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Intellectual disability
autosomal dominant 13
Autosomal dominant cerebellar ataxia
Inborn genetic diseases
DYNC1H1-related disorder
Other Variants in DYNC1H1
rs387906738 rs387906739 rs387906740 rs387906741 rs387906743 rs397509410 rs397509411 rs397509412 rs587780329 rs377669980
Ask Dr. Hemsworth about this variant