RS797044901 DYNC1H1

Health Risk Chr 14:102002694
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Intellectual disability
Charcot-Marie-Tooth disease axonal type 2O
autosomal dominant 13
Intellectual disability
autosomal dominant 13
Inborn genetic diseases
Intellectual disability
Charcot-Marie-Tooth disease axonal type 2O
autosomal dominant 13
Intellectual disability
autosomal dominant 13
Other Variants in DYNC1H1
rs387906738 rs387906739 rs387906740 rs387906741 rs387906743 rs397509410 rs397509411 rs397509412 rs587780329 rs377669980
Ask Dr. Hemsworth about this variant