RS797044918 DYNC1H1

Health Risk Chr 14:102029930
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Intellectual disability
autosomal dominant 13
Charcot-Marie-Tooth disease axonal type 2O
Inborn genetic diseases
Intellectual disability
autosomal dominant 13
Charcot-Marie-Tooth disease axonal type 2O
Other Variants in DYNC1H1
rs387906738 rs387906739 rs387906740 rs387906741 rs387906743 rs397509410 rs397509411 rs397509412 rs587780329 rs377669980
Ask Dr. Hemsworth about this variant