RS766888803 GRIN1
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Associated Conditions
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
Developmental and epileptic encephalopathy 101
autosomal recessive
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
Developmental and epileptic encephalopathy 101
autosomal recessive
Other Variants in GRIN1