RS797044925 GRIN1

Health Risk Chr 9:137163668
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
GRIN1-related disorder
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
Inborn genetic diseases
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
GRIN1-related disorder
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
autosomal dominant
Neurodevelopmental disorder with or without hyperkinetic movements and seizures
Other Variants in GRIN1
rs387906635 rs1554770064 rs797045047 rs797045605 rs141473515 rs145176345 rs146086141 rs869312865 rs878853143 rs200225692
Ask Dr. Hemsworth about this variant