RS779872478 GRIN1

Health Risk Chr 9:137139500
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Associated Conditions
Inborn genetic diseases
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
Other Variants in GRIN1
rs387906635 rs1554770064 rs797044925 rs797045047 rs797045605 rs141473515 rs145176345 rs146086141 rs869312865 rs878853143
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