RS752746786 GNB1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
13 conditions
Intellectual disability
autosomal dominant 42
Myelodysplastic syndrome
7 conditions
Hypotonia
Seizure
Neurodevelopmental Disability
LEUKEMIA
CHRONIC LYMPHOCYTIC
SOMATIC
Neurodevelopmental disorder
Global developmental delay
Neurodevelopmental abnormality
Other Variants in GNB1