RS1554770667 GRIN1
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
autosomal recessive
Intellectual disability
Inborn genetic diseases
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
autosomal recessive
Intellectual disability
Other Variants in GRIN1