RS758432471 GNB1

Health Risk Chr 1:1806513
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What This Variant Does
"CLNSIG=5
Associated Conditions
Seizure
Hypotonia
Neurodevelopmental Disability
Inborn genetic diseases
Autism spectrum disorder
Global developmental delay
Intellectual disability
autosomal dominant 42
Neurodevelopmental delay
Intellectual disability
autosomal dominant 42
Seizure
Hypotonia
Neurodevelopmental Disability
Inborn genetic diseases
Other Variants in GNB1
rs752746786 rs869312826 rs869312825 rs869312824 rs869312823 rs869312822 rs869312821 rs1064795844 rs1135401746 rs771603036
Ask Dr. Hemsworth about this variant