RS869312825 GNB1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
10 conditions
Intellectual disability
autosomal dominant 42
Neurodevelopmental Disability
Seizure
Hypotonia
10 conditions
Intellectual disability
autosomal dominant 42
Neurodevelopmental Disability
Seizure
Hypotonia
Other Variants in GNB1